Uworld Q Flashcards

1
Q

Amatoxins are found In mushrooms and cause what symptoms? Complications? What is the MOA of these toxins?

A

Symptoms start within 6-24 hrs —> abdominal pain, vomiting severe (cholera like diarrhea) Complications? —> hepatic failure or renal failure Potent inhibitors of RNA polymerase 2 (halt mRNA synthesis)

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2
Q

Ricin toxin MOA?

A

Inhibits protein synthesis by cleaning the r RNA component of the eukaryotic 60s subunit

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3
Q

The metabolism of ethanol results in hypoglycemia, this is a result of inhibition of what metabolic process?

What is the reasoning behind this?

A

Gluconeogenesis

Ethanol metabolism by alcohol dehydrogenase & acetaaldehyde dehydrogenase reduced NAD + to NADH. Increases the NADH/NAD+ radio. This inhibits all pathways requring NAD+.

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4
Q

Disease Incidence Definition:

Disease Prevalence Definition:

Which one is dependent on the other and what is the equation?

Case examples:

  1. Improved quality of care would result in what effect on indicidence + prevalence?
A

Incidence is the number of new cases diagnosed in a population in a given time perido

Prevalence is the total number of disease individuals in the population at a particular point.

Prevalence = (indicidence) X (duration of disease)

  1. Increase in just prevalence & constant incidence. Factors that prolong disease duration can increase prevalence because lower mortality in diabetics = more prevalence over time.
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5
Q

Base excision repair is used to _________ induced spontaneously or by exogenous chemicals.

What are the enzymatic steps of this process?

1,2,3,4,5,

A

correct single-base DNA defects

Examples of alterations fixed by DNA repair are depurination, alkylation, oxidation and deamination,

  1. Glycosylase: cleaves altered base leaving AP site
  2. Endonuclease: cleaves 5’ end
  3. Lyase: completes extraction of 3’ sugar-Pi
  4. Polymerase: fills the single nucleotide gap
  5. Ligase: seals the nick
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6
Q

what bacteria causes this?

A

CLOSTRIDIUM Dificile exotoxin B

  • Colonic mucosa responds to toxin exposure by forming white, patch pseudomembranes, which consist of Neutrophil predominant infiltrate, fibrin, bacteria and necrotic epithelium

Pts with severe disease may develop nonobstructive toxic megacolon àleads to perforation (abdominal pain, fever, diarrhea

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7
Q

Key Side effects of Anti Psychotic Drugs:

What are the 3 Extra-Pyramidal side effects? What are the differences between them?

Explain Tardive Dyskinesia

What are the main symptoms of Neuroleptic Malignant Syndrome?

A
  1. Acute Dystonia: Sudden onset, sustained muscle contractions of neck, mouth, tongue or eye muscles
  2. Akathisia: subjective restlessness with inability to sit still
  3. Drug-induced Parksonism: Tremor, Rigidity, Bradykinesia, masked facies

Tardive Dyskinesia: involuntary movements after chronic use (lip smacking, choreoathetoid movements)

NMS: Fever, rigidity, Mental status change, autonomic instability(sympathetic hyper actvity –> sweat, Inc HR)

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8
Q

Exercise Phsyology:

Cardiac Output (Increased/Decreased)

LV-EDP (Increased/Decreased)

Pulmonary A. Systolic P (Increased/Decreased)

Systemic Systolic BP (Increased/Decreased)

Total Systemic Vascular resistance (Increased/Decreased)

A

Cardiac Output (Increased/Decreased)

LV-EDP (Increased/Decreased)

Pulmonary A. Systolic P (Increased/Decreased)

Systemic Systolic BP (Increased/Decreased)

Total Systemic Vascular resistance (Increased/Decreased)

Due to shunting of blood to the muscles

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9
Q

Influenza Vaccine/Pharm:

(Inactivated/ or Live attenuated) vaccine stimulates the formation of neutralizing antibodies agaist hemagluttinin antigen –> preventing viral entry

(Inactivated/ or Live attenuated) vaccines can generate a strong cell-mediated immune response that can kill virally infected cells, in addition humoral immunity.

Oseltamivir MOA

A

Inactivated vaccine stimulates the formation of neutralizing antibodies agaist hemagluttinin antigen –> preventing viral entry

Live attenuated vaccines can generate a strong cell-mediated immune response that can kill virally infected cells, in addition humoral immunity.

Oseltamivir: sialic acid analogue that competively inhbiits influenza neuraminidase –> prevents release of viral progency (virions)

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10
Q

Cavernous Carotid Syndrome

Expanding aneurysm in cavernous portion of ICA will initially cause headache + diplopia.

WHAT ARE THE NERVES THAT ARE AFFECTED BY THIS ?

A

Main one: Abducens Nerve –> Lateral rectus weakness, inward eye deviation

Oculomotor Nerve

Trochlear Nerve

V1 and V2 branches of Trigeminal nerve

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11
Q

Intravenous Fluid & Clinical Indications

Volume resusciation (hypovolemia, shock, sepsis)

Severe, symptomatic Hyponatremia

Free water deficit

Maitenance Hydration

Volume replacement; treatment of SBP or HRS

A

Volume resusciation (hypovolemia, shock)–> 0.9 normal saline or Lactated Ringer solution (both isotonic)

Severe, symptomatic Hyponatremia –> 3% hypertonic saline (hypertonic)

Free water deficit: 5% Dextrose in water or half-normal saline (hypotonic)

Maitenance Hydration: 5% dextrose in half normal saline (hypotonic)

Volume replacement: Albumin (isotonic)

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12
Q

______________ is a blood-loving organism that requires X (hematin) & V (NAD+) factors for growth. This can be accomplished by growing this bacteria in the presence of what? (Satellite phenomenon)

Wont grow on sheep blood’s agar because no factor 5 or 10.

A

Haemophilus influenza

Satellite Phenomenon: Presence of Beta-Hemolytic Staph aureus –> lysis RBCs –> release factor X and V –> growth of Haem infleunza.

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13
Q

Median Nerve Pathway

  1. Arises from the __________ cords of the brachial plexus –> 2. travels in the bicipital groove (w brachial A) –>
  2. Now in the forearm the median nerve courses between the humeral and ulnar heads of the ____________ –>
  3. flexor digitorum profundus –> enter hand through carpal tunnel –> first 3.5 digits (palmar aspect)

Compression at ________ = impaired sensation to palmar aspect of first 3 digits

Compression at _______ = senstaion impaired also to the entire lateral palm + first 3 digits

A

Medial & lateral cords

pronator teres muscle

carpal tunnel

pronator teres

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14
Q

__________ –> episodes of jaundice, impaired bilirubin excretion, black liver, direct bilirubin

_____ Syndrome is also Direct Bilirubine

_____ & _____syndomre = impaired bilirubin conjugation (indirect bilirubinemia)

A

Dubin-Johnson Syndrome:

  • Autosomal Recessive
  • Defective hepatic excretion of bilirubin glucoronides –> mutation in caclilulaur membrane transport protein
  • Episodes of Jaundice (trigger = stress, illness, pregnant)
  • Direct hyperbilirubinemia (because impaired excretion)
  • Liver appears black (gross) due to imapred excretion of epinepherine metabolites (in lysosomes)

Other answers: Rotor; Criggler Najar & Gilbert

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15
Q

____Pancreatic Bud –> Tail, body, most of head, small accesory pancreatic ducts

____pancreatic bud –> Uncinate process, portion of head, proximal portion of main pancreatic duct

________: failure of bentral and dorsal buds to fuse –> pancreatic secretions drained via to seperate duct systems (dorsal draining most)

A

Dorsal Bud

Ventral Bud

Pancreatic divisum

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16
Q

___________complications (name the complication)

  1. Worsening of baseline symptoms + development of painful swallowing

2, Metaplastic columnar epithelium replaces normal stratified squamous –> No change is symptoms, Just dysphagia + weight loss

  1. develops in the setting of healing when collagen fibers contract and cause narrowing of lumen –> feeling of dysphagia + food getting stuck
A

Gastro esophageal Reflux disease (GERD) complications

  1. Erosive esphagitis with esophageal ulcers (odynophagia = painful swallow)
  2. Barret esophagus
  3. Esophageal stricture
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17
Q

WIlson’s Disease results in cystic degneration of what structure?

Huntington disease effects what structure?

What are the other labeled structures?

A

WIlson’s Disease results in cystic degneration of Putamen (B)

Huntington disease effects caudate nucleus (D)

Internal capusle is C

Globus pallidus is D

Amygdala is E

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18
Q

Name the Embryologic malformation & MOA:

  1. Cecum in RUQ, Presense of fibrous bands connecting cecum and right colon to retroperitoneum –> extrinsic compression of duodenum (possible compression of SMA –> necrosis); Present with billious vomiting
  2. Double bubble sign, Billious vomiting, associated with down syndrome
  3. Delayed passage of meconium, abdominal distention, bilious vomit. Mega colon
  4. True Diverticulum, sometimes contains ectopic gastric tissue, rule of 2s
A
  1. Intestinal obstruction & Midgut volvulus due to intestinal marotation
  2. Duodenal atresia due to failure of gut recanilization
  3. Hirschprung disease –> failure of NCC migration in gust –> agagnlionic sigmoid colon/rectum
  4. Meckel Diverticulum
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19
Q

Pulsatile GnRH release from hypothalamus –> stimulate release of LH and FSH from anterior pituitary.

LH stimulates ______ –> release ________

FSH stimulate _______ –> release _______

High Local levels of _______& _______ are necessary for spermatogenesis

A

Theres is a negative feed back loop

Leydig cells –> Release Testosterone

Sertoli Cells –> release Inhibin B

High Local levels of Testosterone & FSH are necessary for spermatogenesis

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20
Q

What gene/protein is defective in familial Dilated cardiomyopathy? Inheritance pattern?

What chemicals can cause Dilated cardiomyopaththy

A

Dilated cardiomyopathy

  • Pathogenesis
    • Direct insult to myocardium –> decrease in contractile function with increase in ventricular cavity size
  • Causes
    • Viral infection
    • Chemicals (Doxorubicin, alchohol, cocaine)
    • Idiopathic/familial (AutoDom) = Truncated TTN gene -> defective Titin protein
  • Symptoms of decompensated heart failure
    • Dyspnea, fatigue, orthopnea
    • Risk of sudden cardiac death due to ventricular arrythmia
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21
Q

Case:3yo Recurrent sinupulmonary infections, giardia lamblia gastreoenteritis, enterovirus infections. Pan-hypoglobulinemia

What disorder is described above? what cell surface (CD) marker would be deficent?

A

X-Linked agammaglobulinemia

  • Mutation in Bruton Tyrosine Kinase à failure of bone marrow pre-B cells to develop into mature B cells (a step necessary for B cells to leave the bone marrow and enter circulation)
  • Recurrent sinopulmonary infections
  • ·Giardia Lamblia Gastroenteritiis
  • ·Failure to thrive
  • ·Low Immunoglobulin levels
  • ·Low or absent B cells (NO cd19,20,21)
  • ·Pan-hypogammaglobulinemia

SCID would be a deficeincy of T and B cells; failure to thrive, candidiasis, severe infections (PCP) at younger age

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22
Q

Atheroembolic disease

  • Typically occurs after an invasive vascular procedure –> mechanical dislodgement of atherosclerotic plaque –> showering of cholestorol-rich emobli into circulation
  • Needle-shaped cholestorol clefts in affected vessels are diagnost
  • Commonly involved organs include
    • ______________________
    • ______________________
    • ______________________
    • ______________________
A
  • Commonly involved organs include
    • Kidneys (Acute Kidney Injury)
    • Skin (blue Toe syndrome, livedo reticularis)
    • GI tract (bleeding, infarction)
    • CNS (stroke, amaurosis fugax)
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23
Q

_________is TB drug that is similar in structure as B6 –> causes B6 deficiency which manifests as:

  • Sensory Ataxia + decreased Pain sensation + numbness and tingling of his hands and feet

_____and _____chemo drugs that inhibit microtubule formation and directly toxic to nerves

A

Isoniazid

Vincristine and Paclitaxel

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24
Q

Type 1 Diabetes Mellitus

  • Hypoglycemia can be induced by:
    • _______________________________
    • ___________________________
    • ____________________________
  • Uptake of glucose by ____________ is mediated by GLUT4 Transporter, which is translocated to the cell membrane in response to _____and/or _________. Hypoglycemia can be precipitated by ______in pts with insulin treated diabetes due to persistent dosing of exogenous insulin.
A

Type 1 Diabetes Mellitus

  • Hypoglycemia can be induced by:
    • Inadvertent overdose of insulin
    • decrease carb intake (skipped meal)
    • Intensive physical exercise
  • Uptake of glucose by skeletal muscle is mediated by GLUT4 Transporter, which is translocated to the cell membrane in response to insulin and/or muscle contraction. Hypoglycemia can be precipitated by exercise in pts with insulin treated diabetes due to persistent dosing of exogenous insulin.
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25
Q

Acute bacterial Prostatis is mostly caused by what organism?

Community acquired pneumonia in endemic areas (califoria, arizon) can also cause erythema nodosum/mulftiforme OR arthralgias?

A

E. Coli

Coccidiodes

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26
Q

Stages of change model (ex: alcohol); what are the 5 stages?

A
  1. Precontemplation
  2. Contemplation
  3. Preparation
  4. action
  5. maintenace
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27
Q

CSF showing Lymphocytic pleocytosis + Acute onset Assymetric flaccid paralysis with concurrent parkinsonias features is highly suggestive of what disease process?

A

West Nile Virus (Flavivirus)

  • Description
    • (+) sense, ssRNA virus
  • Clinical
    • West Nile Fever: headache, rash (maculopapular/morbilliform)
    • Neuroinvasive: meningitis, encephalitis, acute assymetric flaccid paraylysis
      • Parkinsonian Sx (rigidity, bradykineasia, tremor)
  • Transmission
    • Female Mosquitos, summer/fall, Warm climate
  • Risk factors: Older age, malignancy/organ transplant
  • Diagnosis: anti-WNV Abs
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28
Q

Inability to extend wrist on PE. Midshaft fracture of the humerus is found. What structures risk of injury?

A

Humerus fracture associated with inability to extend wrist (wrist drop) indicates radial nerve injury. It innervates most of the forearm extensors(triceps) at the elbow, hand extensors at the wrist, brachioradialis and finger extensors. Consists of c5-T1 nerve roots

Deep brachial A. runs with Radial Nerve posterior to the midshaft of the humerus.

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29
Q

DisordersSerum NaSerum OsmoUrine Osmo

Diabetes Insipidus ??? ??? ???

Primary Polydipsia ??? ??? ???

Diabetes Mellitus ??? ??? ???

SIADH ??? ??? ???

SIADH can be caused by ectopic ADH secreting tumors like ___________________ and head and neck cancers

A

small cell lung carcinoma

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30
Q

Which feature applies to complete hydatidiform mole vs partial?

  1. Enlarged Uterine size
  2. Extremely high ß-HCG
  3. Fetal/Embryonic tissue present
  4. Diffuse trophoblastic proliferation + edematous chorionic villi
  5. Paternal DNA only
  6. p57 positive
  7. Which has higher risk of gestation trophoblastic neoplasia?
A
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31
Q

Complications of Complete Hydatidiform mole?

  • First trimester ______________
  • ______________ (vomiting due to inc ß-hCG)
  • ______________ (due to ß-hCG)
  • Pre-eclampsia, anemia, hyperthyroidism
  • Need to monitor ß-hCG levels after uterine evacuation to risk of malignant transofrmation (______ or __________)
A
  • First trimester vaginal bleeding
  • Hyperemesis gravidarum (vomiting due to inc ß-hCG)
  • Theca-lutein cysts (due to ß-hCG)
  • Pre-eclampsia, anemia, hyperthyroidism
  • Need to monitor ß-hCG levels after uterine evacuation to risk of malignant transofrmation (invasive mole or choriocarcinoma)
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32
Q

________ is a benign, auto recessive disorder. Presents asymptomatic, but urine will test postiive for a reducing sugar (fructose) with copper reduction test. Due to defective _______enzyme.

_________ presents as hypoglycemia & vomitting, after _____ingestion. Complications are failure to thrive, Liver and Renal failure. Due to deficiency of _______ enzyme (failure of __________ –> toxic intermediate). Treat with _________.

_______ is an autosomal recessive disorder due to ________ deficiency. Presents with neonatal jaundice, vomiting, cataracts, hepatomegaly, and failure to thrive. Treat by ________________.

A

Essential Fructosuria is a benign, auto recessive disorder. Presents asymptomatic, but urine will test postiive for a reducing sugar (fructose) with copper reduction test. Due to defective Fructokinase.

Hereditary fructose intolerance presents with hypoglycemia & vomitting, after _____ ingestion. Complications are failure to thrive, Liver and Renal failure. Due deficiency of aldolase B enzyme (failure of fructose-1P metabolism –> toxic intermediate). Treat with elimination of dietary fructose.

Galactosemia is an autosomal recessive disorder due to G-1P uridyl transferase deficiency. Presents with neonatal jaundice, vomiting, cataracts, hepatomegaly, and failure to thrive. Treat by eliminating all milk products and feed soy.

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33
Q

Hep B Serologic Markers

  • ______ –> surface glycoprotein; detectable during acute infection; persistent more than 6 months = chronic infection
  • HBeAg –> Polypeptide; detectable during acute infection; indicates ___________________
  • ___________ –> First sign of acute infection; present during window phase prior to HBsAg & HBeAg
  • _________ –> Seen with cleared infection or vaccination
    • confers long-term immunity
  • Anti-HBe –> develops in cleared infection & later in chronic infection; indicates _________________
  • Anti-HBc IgG –> present in both acute & chronic infection
    • (Present or not present??) after vaccination
A

Hep B Serologic Markers

  • HBsAg –> surface glycoprotein; detectable during acute infection; persistent more than 6 months = chronic infection
  • HBeAg –> Polypeptide; detectable during acute infection; indicates viral replication & infectivity
  • Anti-HBc IgM –> First sign of acute infection; present during window phase prior to HBsAg & HBeAg
  • Anti-HBs –> Seen with cleared infection or vaccination
    • confers long-term immunity
  • Anti-HBe –> develops in cleared infection & later in chronic infection; indicate Dec viral replication/infectivity
  • Anti-HBc IgG –> present in both acute & chronic infection
    • Not present after vaccination
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34
Q

Precision(_____) definition

Accuracy(____) definition.

A

Precision(reliability) = ability of test to reproduce identical or similar results with repeated measurements

Accuracy(validity) = ability of a test to measure what it is suppose to measure. For a new test to be accurate it results should be equivalnt to the results obtained with a gold standard on the same individual.

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35
Q

Just compare these TWO

Hereditary fructose intolerance.

  • Aldolase B deficiency (Life threatening disorder)
  • Patients present with fructose containing foods are introduced into the diet. (baby weaned off breast milk onto a fructose containing product)
  • Vomiting and hypoglycemia 20-30 mins after fructose ingestion. Hypoglycemia is a result of intraceullar accumulation of fructose 1-phoshohate and depletion of inorganic phosphate –> inhbiition of glycogenolysis and gluconeogenesis.
  • Failure to thrive, jaundice and hepatomegaly
  • Complications: Liver failure and renal failure –> death
  • Tx: fructose free diet
A

Classic Galactosemia

  • Galactose-1P uridyl transferase deficiency (life threaten)
  • Autosomal recessive
  • Vomiting, feeding intolerance, neonatal jaundice, hepatomegaly and death if untreated
  • Symptoms start soon after breast feeding initiated (younger age)
  • Neonatal cataracts?
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36
Q

Tumbling motility is pathomnemonic for?

A

Listeria monoctyogenes (unpasteurized milk)

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37
Q

25-hydroxylase (in Liver)

1 alpha-hydroxylase in Kidney

A
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38
Q

Fluid movement across the capillary wall (filtration) into the interstitium is dependent on (1) hydrostatic pressure, (2) oncotic pressure and (3) capillary permeability. It is tighly balanced by lymphatic drainage (returns interstitial fluid to the vasculature. Peripheral Edema results when transcapillary plasma filtration exceeds the resorptive capactiy of the lymphatics

Factors that favor development of edema include:

  • Elevated capillary hydrostatic pressure
    • Arteriolar dilation or impaired venous return
  • Decreased plasma oncotic pressure
    • Decreased albumin (nephrotic syndrome, cirrhosis, malnutrition)
  • Sodium and water retention
    • Lowers oncotic pressure & inc hydrostatic pressure
    • kidney Disease and heart failure
  • Lymphatic obstruction
    • Filiariasis, invasive malignancies, iatrogenic (surgical LN dissection and radiation therapy)
A

JUST GET FAMILIAR WITH THIS SHIT

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39
Q

Tricyclic antidepressants (TCAs) side effects

  • Inhibition of NT(NE & 5-HT) reuptake –> Tremor & insomnia
  • Blockade of cardiac fast sodium channels –> Conduction defects, _______, _______
  • Antagonism of Muscarinic Ach-R –> _______, dry mouth, _________, hyperthermia, _____ RETENTION
  • Antagonism of alpha-1 adrenergic receptors –> ______
  • Antagonism of H1 receptors –> ____
A

SNRI

· Selective inhibits presynaptic Re-uptake of Serotonin (via SERT AND Norepinephrine (via NET)

Includes TCAs

·3°Amine TCA: inhibit both 5HT & NE relatively equally

·2°Amine TCA:inhibit NE> 5HT

Normal SNRI:

  1. Desvenlafaxine
  2. Duloxetine
  3. Venlafaxine
  4. Levomilnacipram

TCAs

5.3°Amine TCA:

Amitriptyline

Clomipramine

Doxepin

imipramine

6.2°Amine TCA

Amoxapine

Desipramine

Nortriptyline

SNRI’s + DA

Amoxapine

TCAs also block other receptors (side effect)

·ONLY TCA based SNRI have impact on 3 key non-efficacy related receptors

1.Histamine (H1)

2.Muscarinic(cholinergic)

3.a1 adrenergic

TCA system based-side effects(toxicity)

1.Cardiovascular (a-adrenergic)

-Tachycardia, orthostatic Hypotension, dysrhythmias(life-ending)

2. Anticholinergic (muscarinic)

-Dry mouth, urinary retention, constipation, Blurred vision, increase IOP

3. CNS (histamine)

-Sedation/fatigue & dizziness/seizures

TCA: Toxic ingestion overdose

3Cs:

  1. Coma
  2. Cardiotoxicity (conduction abnormalities) – Quinidine-like (slows conduction and phase 0 depolarization (class1A))
  3. Convulsions

Rest of the SNRIs have similar side effects to SSRI

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40
Q

Acyclovir, valacyclovir, Famciclovir, Ganciclovir

  • _______ analog
  • Once it enters the host cell it is phosphorylated to acyclovir-monophosphate by a ______-encoded _________ (RATE LIMITING STEP) in acyclovir activation –> then phosphorylated by _____ enzymes to active Triphosp form –> impairs DNA polymerase mediated replication of ________
  • Effective against _________ and __________
  • ______ and ______do not produce the same thymidine kinase –> less effective
A

cyclovir, valacyclovir, Famciclovir, Ganciclovir

  • Guanosine analog
  • Once it enters the host cell it is phosphorylated to acyclovir-monophosphate by a virally-encoded thymidine kinase (RATE LIMITING STEP) in acyclovir activation –> then phosphorylated by cellular enzymes to active Triphosp form –> impairs DNA polymerase mediated replication of HSV/VZV
  • Effective against Herpes Simplex and Varicella Zoster
  • CMV and EBV do not produce the same thymidine kinase –> less effective
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41
Q

Chronic Kidney Disease leads to ________________and causes hypocalcemia –> which manifests as:

  • Chvostek (__________________________________)
  • Trosseau (____________________________________)
  • _____________reflexia
  • QTc _______________________
  • Seizures
A

Chronic Kidney Disease leads to hyperphosphatemia and causes hypocalcemia –> which manifests as:

  • Chvostek (facial twitiching elicited by tapping of Facial N)
  • Trosseau (carpal spasm triggered by inflation of BP cuff around the arms)
  • HYPERreflexia
  • QTc prolongation
  • Seizures
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42
Q

Lidocaine is a _____________ that blocks transmission from free nerve endings. It is mised with epinephrine which causes __________________ when injected SQ. This ______________________, decreases bleeding during the procedure and reduces sytemic lidocain absorption.

A

Lidocaine is local anesthetic that blocks transmission from free nerve endings. It is mised with epinephrine which causes profound vasoconstriction when injected SQ. This prolongs lidocaine’s duration of action, decreases bleeding during the procedure and reduces sytemic lidocain absorption.

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43
Q

Antibiotics and there MOA

  1. ___–> prevent production of UDP-NAM by blocking MurA
  2. Beta Lactams –> prevent ________of peptidoglycan
  3. _______–> prevents subunit incorporation
  4. _________& ________inhibit bacterial 50s subunit; __________=>myelosuppression+aplastic anemia
  5. flouroquinolones(ciprofloxacin) –> inhibit ________ and _____________
  6. ________–>inhibit 30s sub unit (protein synth)
A

Antibiotics and there MOA

  1. Fosfmyocin –> prevent production of UDP-NAM by blocking MurA
  2. Beta Lactams –> prevent transpeptidation of peptidoglycan
  3. Vancomycin –> prevents subunit incorporation
  4. Azithromycin & chloramphenicol inhibit bacterial 50s subunit; chloramphenicol=>myelosuppression+aplastic anemia
  5. Flouroquinolones(ciprofloxacin) –> inhibit DNA topoisomerase and gyrase (DNA damage)
  6. Doxycline –>inhibit 30s sub unit (protein synth)
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44
Q

Collagen subtypes

  • Type __ –> Basement membrane
    • Alport syndrome
  • Type 1 –> ___, dermis, ____, _____, dentin, cornea, blood vessels & ______tissue
    • (what disorder associated)
  • Type _ –> Skin, ______, intestines, _____vessels, bone marrow, _______, & _______tissue
    • Ehlers-Danlos Syndrome
  • Type 2 –> _______, vitreos humor, & __________
    • _______
A

Collagen subtypes

  • Type 1 –> Bone, dermis, tendons, ligaments, dentin, cornea, blood vessels & scar tissue
    • Osteogenesis impefecta
  • Type 2 –> Cartwolage, vitreos humor, & nucleus pulposus
    • Nothing
  • Type 3 –> Skin, lungs, intestines, blood vessels, bone marrow, lymphatics, & granulation tissue
    • Ehlers-Danlos Syndrome (3&4)
  • Type 4 –> Basement membrane
    • Alport syndrome
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45
Q

Time after Myocardial Infarction —> Light microscopy change

0-4 hours —> _______

4-12 hours–> wavy fibers with ____, ______mycoytes

12-24 hrs–>Myocyte hyper______ w ______(shrunk) nuclei

1-3 days–>____________(loss of nuclei/striations), predominately _______ infiltrate

3-7 days–> Disintegration of dead ___ & myofibers; _________infiltration at border areas

7-10days–> Robust phagocytosis of dead cells by __; beginning of _________ formation at margins

10-14 days–> well developed ______tissue w _________

2wks-2months–> Progressive _________and ____ formation

A

ime after Myocardial Infarction —> Light microscopy change

0-4 hours —> No change

4-12 hours–> wavy fibers with narrow, elongated mycoytes

12-24 hrs–>Myocyte hypereosinophilia w pyknotic(shrunk) nuclei

1-3 days–>Coagulation necrosis(loss of nuclei/striations), predominately neutrophil(Nø) infiltrate

3-7 days–> Disintegration of dead Nø & myofibers; macrophage infiltration at border areas

7-10days–> Robust phagocytosis of dead cells by Mø; beginning of granulation tissue formation at margins

10-14 days–> well developed granulation tissue w neovascularization

2wks-2months–> Progressive collagen deposition and SCAR formation

NEED TO ADD POST MI COMPLICATIONS in here

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46
Q

CytoMegalo Virus (CMV)

  • Herpes family, enveloped dsDNA virus
  • Most are asymptomatic
  • High risk patients for serious infection are
    • Transplant pts, HIV pts, and fetuses
  • Histology shows intranuclear and intracytoplasmic inclusions; often have a surrounding halo (Owl’s eye)
  • HIV pts complications: Esophagitis, colitis Retinitis
  • Transplant patients –> pneumonitis
A

CytoMegalo Virus (CMV)

  • Herpes family, enveloped dsDNA virus
  • Most are asymptomatic
  • High risk patients for serious infection are
    • Transplant pts, HIV pts, and fetuses
  • Histology shows intranuclear and intracytoplasmic inclusions; often have a surrounding halo (Owl’s eye)
  • HIV pts complications: Esophagitis, colitis Retinitis
  • Transplant patients –> pneumonitis
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47
Q

__________poisoning_

  • Findings: Reddish skin discoloration, lactic acidosis, hypertension, narrowing of venous arterial PO2 gradient
  • Complications quickly develop: CV collapse & seizures
  • Targets cytochrome C oxidase in mitochondria
  • Toxicity of _______is dependent upon its ability to bind ferric iron(Fe3+) with high affinity affinity
  • Antidotes
    • inhaled amyl nitride –> what is MOA?
    • Hydroxycobalamin
A

Cyanide poisoning

  • Findings: Reddish skin discoloration, lactic acidosis, hypertension, narrowing of venous arterial PO2 gradient
  • Complications quickly develop: CV collapse & seizures
  • Toxicity of cyanide is dependent upon its ability to bind ferric iron(Fe3+) with high affinity affinity
  • Antidotes
    • inhaled amyl nitride
      • Convert Fe2+ in Hemoglobin to Fe3+ –> makes Methemoglobin (binds cyanide with high affinity) –> sequesters cyanide and protects it from effecting Mitochondrial cytochrome C oxidase)
    • Hydroxycobalamin
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48
Q

Eukaryotic Gene Transcription Mediators

Promoter sequence:

  • Directly Bind Transcription Factors and RNA polymerase II ________from the gene locus.
  • This is ____________ for initation of transcription
  • Examples: ____(Hogness box:25 bases upstream) or ___box(70-80 bases upstream)

Enhancer/Silencer Sequence

  • Bind activator proteins that facilitate ______ of DNA. Which allows activator proteins to interact with TFs and RNA poly2 @ ________site –> increases rate of transcription(or decrease by binding repressors if silencer)
  • Can be __________ from gene locus and can be near gene locus or very far away. Can also be within ____as well as on ________chromosomes
A

ukaryotic Gene Transcription Mediators

Promoter sequence:

  • Directly Bind Transcription Factors and RNA polymerase II upstream from the gene locus.
  • This is necessary for initation of transcription
  • Examples: TATA(Hogness box:25 bases upstream) or CAAT box(70-80 bases upstream)

Enhancer/Silencer Sequence

  • Bind activator proteins that facilitate BENDing of DNA. Which allows activator proteins to interact with TFs and RNA poly2 @ promoter site –> increases rate of transcription(or decrease by binding repressor if silencer)
  • Can be upstream or downstream from gene locus and can be near gene locus or very far away. Can also be within introns as well as on seperate chromosomes
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49
Q

Traveler’s Diarrhea is most commonly due to ETEC. This pathogen produces plasmid-encoded, heat-labile(LT or cholera-like toxin) and heat stabile toxin(ST) enterotoxins

LT activates _______cyclase –> Inc _____

ST activates ______cyclase –> inc ______

Both cause water, electrolyte loss and waterry diarrhea and some abdominal pain

A

Traveler’s Diarrhea is most commonly due to ETEC. This pathogen produces plasmid-encoded, heat-labile(LT or cholera-like toxin) and heat stabile toxin(ST) enterotoxins

LT activates adenylate cyclase –> Inc cAMP

ST activates guanylate cyclase –> inc cGMP

Both cause water, electrolyte loss and waterry diarrhea and some abdominal pain

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50
Q

OCD first line treatment is ?

A

Selective Serotonin Reuptake inhibitor

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51
Q

Blood brain barrier is made of _______________which associate with actin filaaments to form a belt-like seal.

______are spot like junctions that anchor adjacent cells together via keratin intermediate filaments. (site of pemphigus vulgaris Abs)

_____________ permit free passage of small ions/molecules

_______bind basal layer of epithelial cells to basemment membrane (Bullous pemphigous Abs)

_________________ right below tight juctions

A

Blood brain barrier is made of Tight Junctions (zona occludens: claudins & occludins) which associate with actin filaaments to form a belt-like seal.

Desmsomes are spot like junctions that anchor adjacent cells together via keratin intermediate filaments. (site of pemphigus vulgaris Abs)

Gap junctions (connexins) permit free passage of small ions/molecules

Hemidesmosomes bind basal layer of epithelial cells to basemment membrane (Bullous pemphigous Abs)

Intermediate junctions (zona adherens) right below tight juctions

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52
Q

(Rotavirus or Norovirus?)

is the most common cuase of viral gastroenteritis. Outbreaks are common and symptoms include vomiting and watery diarrhea.

A

Norovirus

there is a rotavirus vaccine in developed coutnries so it is unlikely

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53
Q

Which cardiac tissue has the slowest conduction velocity?

Which cardiac tissue has the Fastest conduction velocity?

Think of the mnemonic

A

Slowest= AV node

Fastest =Purkinje system

AV node, Ventricular muscle, Atrial Muscle, Purkinje System

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54
Q

Myotomes of the upper extremity(which spinal number?)

  • Shoulder/scapula elevation —> ______
  • Finger abduction —> _____
  • Shoulder abduction –> _____
  • Wrist Flexion & Finger Flexion –> _____
  • Elbow flexion & wrist extenion –> ______
  • Elbow extension & Finger extension –> ______
A
  • Shoulder/scapula elevation —> C4
  • Finger abduction —> T1
  • Shoulder abduction –> C5
  • Wrist Flexion & Finger Flexion –> C8
  • Elbow flexion & wrist extenion –> C5, C6
  • Elbow extension & Finger extension –> C7
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55
Q

Reflexes of Upper extremity (What spinal level?)

  • Biceps + Brachioradialis => _____
  • Trceps => _____
A
  • Biceps + Brachioradialis => C5, C6 (musculocutaneous N._
  • Trceps => C7, C8
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56
Q

What surface marker is specific to the monocyte/Macrophage lineage?

A

CD14

This question came in the context of epitheliod histiocyte in caseating granuloma of TB

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57
Q
  1. In acute compartment syndrome (after post-ischemic reperfusion injury), reactive oxygen species are formed due to high oxidative stress. Which enzymes can help neutralize these damaging species?

Deficiency of what enzyme leads to Chronic granulomatous disease?

A
  1. Antioxidants: Superoxide Dismutase, Glutathione Peroxidase, Catalase

2, NADPH oxidase

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58
Q

What is the difference between the following 3 categories of microbiology mediums? What are examples of each?

Differential Media

Enrichment media

Selective Media

A
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59
Q

In a normal distribution (bell shaped curve) Median, mode and mean are all equal.

  1. In a postively skewed plot in which order (highest to lowest) are these 3 found in?
  2. In a Negatively skewed plot in which order (highest to lowest) are these 3 found in?
A

Positve: Mean(highest), median, mode

Negative: Mode(highest), median, Mean

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60
Q

Can a Turner Syndrome patient get pregant? (yes or no)

A

Yes: ONLY by. In Vitro Fertilization is possible in Turner Syndrome patient

Look at other

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61
Q

Which of the following is the last structure to disappear as you descend through the respiratory tract?

Cartilage

Cilia

Goblet cells

Mucous glands

Serous glands

A

Cilia is correct (present in respiratory bronchioles in order to serve function as mucociliary escalator. Take note that the airway epithelium cahnges for pesudostratified ciliated columnar to cilaited simple cuboidal by the level of terminal bronchioles.

Bronchololes lack glands and cartilage and levels of goblet cells decrease as you get more distal. But cilia are the last ones at the level of respitaory bronchioles

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62
Q

____________ is an autosomal recessive disorder caused by mutation in the BLM gene of ______–> chromosamal instability and breakage.

Clinical manifestation is growth retardation, facial anomalies, photosensitive rash, and immunodeficiency

A

Bloom Syndrome is an autosomal recessive disorder caused by mutation in the BLM gene of helicase –> chromosamal instability and breakage.

Clinical manifestation is growth retardation, facial anomalies, photosensitive rash, and immunodeficiency

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63
Q

What structures are derived from the 3rd pharyngeal pouch?

What structures are derived from the 1st pharyngeal pouch?

A

Thymus and inferior parathyroids

Epithelium of middle ear and audotory tube

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64
Q

PSGN shows granular deposits of ___, ___, and ____ in the mesangium and basement membrane.

A

IgG, IgM and C3

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65
Q
  1. What are the ultrasound findings of Down Syndrome?
  2. What is the genetic cause of this condition?
  3. What is GI manifestation is associated with this condition?
A
  1. Decreased Materenal serum alpha-fetoprotein AND increased nuchal translucency
  2. Mostly due to meiotic non disjunction
  3. Duodenal atresia (double bubble)
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66
Q

Open neural tube and ventral wall defects are associated with what key lab finding in utero?

Holoprosencephaly is most associated with which congential trisomy?

A

Markedly elevated AFP are associated with open neural tube (spina bifida) and ventral wall defects(gastroschisis &omphalacele)

Trisomy 13 (Patau)

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67
Q

What is the function of IL-2? IL-4? TNF-alpha?

A
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68
Q

Incidence vs prevalence?

A
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69
Q

What microtubule associated protein is involved in anterograde transportion of materials and cells? What about Retrograde?

Which one does the reactivation of Herpes Simplex virus use?

A

HSV reactivation uses kinesin

HSV initial infection used dynein to become latent in ganglia

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70
Q

Mullerian Duct Anomalies:

  1. Failure of Lateral fusion of the paramesonephric ducts results in?
  2. Complete Agenesis of Paramesonephric duct results in?
  3. Involution of the paramesonephric duct?
  4. What other anomalies are commonly associated?
A
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71
Q

What is the function of IL-1, IL-5, IL-12, Interferon gamma, TNF alpha, IL-10, TGF-Beta, IL-4, IL-17, IL-12? Which ones are anti-inflammatory?

A
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72
Q

What is the pathophysiology of Non-typhoid salmonella vs Salmonella Typhi?

What is the difference in clinical presentation?

A
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73
Q

SMA syndrome is caused by what? and compresses what particular portion of the small intestine?

Presents with billious vomitting

A
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74
Q

Folate is tied to nucleotide synthesis via which enzyme?

In a folate deficient state, supplementing what substance can help limit the amount of cells undergoing apoptosis? In other words which substance can mask the symptoms of folate deficiency?

A

Thymidalate synthesis

Thymidine

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75
Q

Interscalene nerve block is used to provide anesthesia for what body parts?

What is at risk of transient paraylysis via what nerve?

A

Shoulder and upper arm (C5-C7)

Diaphragm (C3-5; phrenic nerve)

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76
Q

Describe the following studies:

Case-control study

Cohort study

Cross-sectional surveys

Ecologic Study

Qualitative study

Nested case control study?

Systematic Review?

A
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77
Q

What are the two most common alternative opioid agonists used for opioid withrawal and craving?

Which on is a full-mu-opioid receptor agonist and is known for its long-half life?

Which one is a partial agonist, less likley to cause respiratory depression?

A

Methadone (used with nalaxone) and buprenorphine

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78
Q

Erythrocytosis can be defined as hematocrit greater than ___ in men and ___ in women.

Measurement of _______ is needed to distinguish absolute from relative.

A

52% and 48&

RBC mass

normal RBC mass indicates what cause? (look up)

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79
Q

Mitochondrial Diseases

  1. Known to have what inheritance? Do they effect boys or girls more?
  2. What is the name for the variable degrees of severity season in mitochondrial disease? What is the reason behind this variability?
A
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80
Q

Mitochondrial syndrome:

  1. (NAME) leads to bilateral vision loss
  2. (NAME) myoclonic seizures and myopathy associated with exercise. Skm biopsy shows irregulary shaped muscle fibers.
  3. (NAME) seizure disorder several stroke like episodes with neurologic deficits. Muscle weakness. Increased lactate and rest and post exercise)
A
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81
Q

Name the associated E.coli virulence factor and MOA?

  1. Bacteremia and septic shock
  2. Neonatal meningitis
  3. Gastroenteritis (blood)
  4. Gastroenteritis (watery)
  5. UTI
A
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82
Q

____________ is characterized by episodic, spontaneous (during rest and nighttime) with transient ST elevation due coronary vasospasm.

What could be some aggravating factors?

What is the Treatment for this?

A

Prinzmental (variant) angina is characterized by episodic, spontaneous (during rest and nighttime) with transient ST elevation due coronary vasospasm.

Dihydroergotamine, cigarette, cocaine/amphetamine, triptans

Vasodilators like Nitroglycerin or CCBs

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83
Q

What is the biggest Risk Factor for Renal Cell Carcinoma?

What is a familial Gene mutation associated with RCC?

A

Smoking

Von Hippel Lindau gene (AD also hemagioblastoma + pheochromacytoma)

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84
Q

What is the mnemonic for TB drugs?

Which one’s MOA is inhibition of Arabinosyl transferase?

Which one causes red-orange body fluids and cytopenias?

Which one causes hepatotoxicity and hyperuricemia?

Which one’s MOA is inhibition of mycolic acid synthesis?

Which one causes Optic Neuropathy?

Which one requires B6/pyroxidine as a supplement?

A

R.I.P.E.

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85
Q

Which antibiotics act on the 50s subunit?

Which act on the 30s subunit?

A

50S: chloramphenicol, clindamycin, linezolid, macrolides

30s: tetracycline, doxycycline, amingoglycosides

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86
Q

Antibiotics that inhibit cell wall synthesis.

(NAME) prevents production of UDP-NAM via inhibition of MurA

(Two classes of drugs) are _____ that bind to and inhibit transpeptidase

(Name) binds to the D-alanine-D-alanine terminus of peptidoglycan –> preventing cross linking

A

Fosfomycin

Penicillin and cephalospirin

Vancomycin (D-alanine substituion to D-lactate is method of resistance)

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87
Q

Teratogenic medications: Contraindicated in pregnancy

  1. Phenytoin –>
  2. Lithium –>
  3. Valproate –>
  4. Isotretinoin –>
  5. Methotrexate –>
  6. ACE- inhbitor –>
  7. Warfarin –>
A
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88
Q

Thiamine Deficiency results in which two syndromes?

A

Wernicke-Korsakoff and Beri Beri

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89
Q

Wernicke Korsakoff manifests as _____, ______, _______and _________________. Occurs Primary in _________ –> ______deficiency.

Infantile Beriberi appears at age ______. Manifests as fuliminant ___________________.

A

Wernicke Korsakoff manifests as confusion, ataxia, oculomotor abnormalites and permanent memory deficits. Occurs Primary in alcoholics. Thiamine deficient.

Infantile Beriberi appears at age 2-3 months. Manifests as fuliminant cardiac syndrome (cardiomegaly, tachycardia, Cyanosis, dyspnea, vomitting)

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90
Q

Adult Beriberi is associated with a deficiency in what?

How does Dry Beriberi manifest and how does it differ from Wet Beri Beri?

A

Dry Beriberi = symmetric peripheral neuropathy of the distal extremities with resulting sensory + motor impairment.

Wet Beriberi = the addition of CARDIAC involvement (cardiomyopathy, high output congestive HF, peripheral edema, tachycardia)

CNS involvement is mostly just Wernicke Korsakoff syndrome (alcoholics)

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91
Q

Vitamins and there primary function!

B1(thiamine) –> _______

B2(riboflavin) –> ____________________

B3(Niacin) –> ________________

B6(pyridoxine) –> ____________________

B9(folate) –> ____________________________

B12(cobalamin) –> _____________________

Vit C (ascorbic acid) –> __________________________

A

Vitamins; NOW TELL ME THE ASSOCIATED deficiency!!

B1(thiamine) –> Decarboxylation of alpha keto acids

B2(riboflavin) –> Mitochondrial electron carrier (FMN, FAD)

B3(Niacin) –> Electron transfer reactions (NAD/NADP)

B6(pyridoxine) –> Transamination of Amino acids (AA synthesis)

B9(folate) –> Hydroxymethyl/formyl carrier (purine & thymine synthesis)

B12(cobalamin) –> isomerase & methyltransferase co factor (DNA & methionine synthesis)

Vit C (ascorbic acid) –> Hydroxylation of proline and lysine (collagen synthesis)

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92
Q

Which cells play a role in COPD?

Which Cells play a role in asthma?

A

COPD –> Neutrophils (elastase), Macrophages and CD8+ T lymphocytes

Asthma–> CD4+ Helpers, Eosinophils. Mast cells?

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93
Q

M1 receptors are found in ?

M2 Receptors are found in ?

M3 Receptors are found in ?

A

M1 receptors are found in the Brain (Memory/cognitive function)

M2 Receptors are found in heart(dec HR + atrial contraction)

M3 Receptors are found in:

  • Lungs (Bronchoconstriction),
  • Bladder (Detrusor contraction),
  • Eyes(Pupillary sphincter contraction–> Miosis, ciliary muscle contraction–> accomodation),
  • GI(Inc peristalsis, salivary secretion and gastric secretion)
  • Skin (increased sweat production) and
  • Peripheral vasculature (Smooth muscle relaxation [via NO] –> vasodilation, hypotension)
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94
Q

Explain the mechanism of activation of M3 receptors on peripheral vasculature.

Explain M3 receptors activation in other locations

A

M3 receptors are present on endothelial cells. Activation leads too production of Nitric Oxide –> diffuses into vascular smooth muscle –> activate Guanylate cyclase –> inc cGMP –> myosin light chain phoshphatase –> dephosphorylates myosin and prevents interaction of myosin head with actin –> smooth muscle relaxation and vasodilation.

GPCR–> inc calcium –> smooth muscle contraction

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95
Q

Primary osteoporosis lab values:

  • Calcium: (Increased/Decreased/normal)
  • PTH (Increased/Decreased/normal)
  • Phosphorous (Increased/Decreased/normal)

Risk factors for osteoporosis

  • Nonmodifiable
    • ???
  • Modifiable
    • ????

Presentation

  • ____fractures, ___fractures
A

Primary osteoporosis lab values:

  • Calcium: (normal)
  • PTH (normal)
  • Phosphorous (normal)

Risk factors for osteoporosis

  • Nonmodifiable
    • Advancing age, Female, White/hispanic/asian, Fam Hx
  • Modifiable
    • Dec Physical activity, Low body weight, poor Ca2+/VitD, alcohol or tobacco use, Premature Menopause, Glucorticoid use

Presentation

  • Vertebral fractures, Hip fractures
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96
Q

Progressive Multifocal leukoencephalopathy is caused by what Virus?

When does initial infection occur?

What cells does this virus attack?

How does this present and in what kind of state?

Brain MRI findings?

A

JC polyoma virus reactivation

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97
Q

EBV virus encephalitis in AIDS can cause__________ which presnts as a signle enhancing lesion

A

primary CNS lymphoma

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98
Q
  1. What LN does the testis drain to?
  2. Scrotum? what other structures drain to this common LN
  3. Glans Penis?
  4. What strucutures does the Inferion Mesenteric node drain?
A
  1. All lymph from ubilicus to the feet, including external genitalia and anus (up to the dentate line); except testis, glans penis and cutaneous posterior calf.
  2. descending and sigmoid colon and upper rectum
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99
Q

Right-sided brachiocephalic vein obstruction

Can be caused by ?

Presents as ?

What is the difference between this and SVC syndrome?

A

Apical Lung tumor compression or catheter

Right sided face, and arm swelling/redness. Engorgement of SubQ veins on same side of neck.

SVC syndrome is the exact same except BILATERAL

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100
Q

Male patient with Nocturnal Back pain, spinal tenderness and indurated prostate suggests what diagosis?

Leuprolide therapy is initated what would be the effect on Testosterone and DHT?

A

Prostate Adenocarcinoma

In Normal physiology GnRH is released in a pulsatile fashion( 90-120 mins) to stimulate LH release –> stimulate androgen production.

In this medical orchiectomy, leuprolide (GnRH analog) is given in continous fashion instead –> this will eventually lead to downregulation of of GnRH receptor on pituitary –> lower LH –> lower Testosterone and DHT

However initally, there is a transient increase in systemuc androgens during first week of therapy

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101
Q

What is the main function of M protein the virulence factor of Strep pyogenes ?

M protein shares strucutral homology with what?

A

Resist phagocytosis

Tropmyosin and myosin –> rheumatic carditis

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102
Q

Oxygen supplementation in premature infants can lead to what eye maninfestaton? What growth factor is used? what are the complications of this?

A

Retinopathy of prematurity or renrolental fibroplasia

VEGF

Retinal vessel neovascularization –> retinal detachment and blidness

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103
Q

Sharp Chest pain that radiates to left shoulder. Pain increases with inspiration and is partially releived by sitting up and leaning forward. What is the diagnosis? what would be an additional finding on PE?

A

Acute pericarditis and pericardial friction rub is an exam finding (scratching sound)

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104
Q

Which adregenic drugs are known to cause orthostatic hypotension?

What are the effects of B2 agonism?

A

alpha 1 antagonist

B2 stimulation –> bronchodilation, vasodilation in SKM, uterine relaxation

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105
Q

The Progression of Diabetic nephropathy can be reduced by glycemic control and ______________? By what mechanism?

A

ACE inhibitors (prils) –> lowers glomerular pressure (antiproteinuric effect)

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106
Q

Which Diabetes Drug class works by activating peroxisome proliferator activated receptor gamma?

What are the metabolic effects of activating this receptor?

A

Thiazolidinediones (TZDs)

Decreases insulin resistance by upregulating GLUT4 in adipocytes and SKM & upregulating adinopectin release by fat tissues.

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107
Q

How can you test which pupil has the lesion in aniscoria?

A
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108
Q
  1. What is the treatment for ganciclovir resistant CMV? Hint: This alternative drug causes hypocalcemia and hypomagnesia
  2. Which CMV drug is associated with nephrotoxicity (proteinuria + inc Cr)?
  3. What side effects does gangciclovir cause?
A

1.Foscarnet ( it can also chelate calcium and induce renal wasting of Mg)

Side note: Low Ca OR Low Mg cna both promote seizures

2. Cidofuvir

3. Severe neutropenia

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109
Q

Gastric Bypass leads to small intestinal bacterial overgrowth (SIBO) –> this leads to an elevation what subtances?

A

Vitamin K and Folate (produced by enteric bacteria) –> N/V/D + malabsoprtion of pther nutrients(B12, A, D, E) due to bypass

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110
Q

Abrupt onset of sudden severe headache indicates what

A

Rupture of berry saccular aneurysm –> subarachnoid hemorrhage

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111
Q
A
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112
Q

Highest risk factors of abdominal aortic aneurysm?

A

Male + smoking and age greater than 65

AA involves transmural inflammation

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113
Q

What does the SADPUCKER nmenonic stand for? is SPleen one of them?

A
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114
Q

What does the POWER of s study indicate?

Is POWER related to type 1 or 2 error?

Define a Type 1 vs Type @ error

A

Ability of a study to detect a dfiference beween groups when such a difference truly exists.

Type 2 error (B) (Power = 1 -B)

Type 1 error (alpha) –> described probablty of seeing a difference when there is no difference in reality. Alpha = probababilily that the observed difference is due to chance alone.

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115
Q
  1. One or more deep, painful ulcers with ragged borders that have grey exudate, inguinal LAD. Immigrant. Gram negative rod in clumping pattern. WHat is the organism?
  2. Multiple, small, grouped ulcers, shallow with erythematous base. Multinucleated giant cells + intranuclear inclusions? Painful.
  3. Extensive & progressive ulcerative lesions without LAD. Deeply staining, gram-negative intracytoplasmic cysts?
  4. Single, indurated, well circumscribed ulcer with clean base.
  5. Small and shallow ulcers. Large, painful, coalesced inguinal LNs. Intracytoplasmic chlamydial inclusion bodies in epithelial cells and leukocytes.
A
  1. this is a chancroid (Haempholis Ducreyi)
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116
Q

Can you explain how low body weight, frequent strenous exercise, chronic illness, eating disorders contribute to functional amenorrhea?

A

FHA is due to reduced circulating leptin (due to diminished adipose tissue) –> inhbiit pulsatile gonadotropin releasing hormone from hypothalamus –> dec LH and FSH –> Low Estrogen –> amenorrhea

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117
Q

What is the first line treatment for acute gouty arthritis?

If the patient has PUD or Renal failure what is the second line treatment for acute goutry arthritis? What is the MOA

A

NSAIDs

Colchicine –> disrupts microtubule formation

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118
Q

Sudden upward jerking of the arm at the shoulder can injure ______. Leading to Difficulty performing fine finger movements.

A

Lower Trunk of Brachial Plexus (Median and ulnar nerves) –> total hand claw deformity (Klumpke claw)

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119
Q

Vasectomy involves transection of the vas deferens. What should the patient be advised against and why?

A

unrprotected sex because viable sperm can still be present in distal vas deferns for 3 months or 20 ejeculations afterward.

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120
Q

Volar lunate dislocation can can compress/injure what nerve?

Hook of hamate fracture?

A

Median Nerve

Ulnar Nerve

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121
Q

What are the findings in Late teriary syphillis?

A

Gummas. Neurosyphillis, ascending aortic aneurysm, aortic valve insufficiency

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122
Q

An infant with poor feeding, vomiting and progressive lethargy. Diaper has Burnt sugar smell. Normal pregnancy and Delivery. Other children are healthy. Mom has exclusively breast fed. Infant has Dry Mucous membranes and generalized Hypertonia.

What is diagnosis? What Enzyme is deficient? What Should you restrict from this patients diet? what is the treatment?

A

Maple Syrup Urine disease

  • Autosomal recessive
  • Branched alpha keto acid complex deficiency
    • Needed to Break down of Leucine, Isoleucine and Valine to go into TCA cycle
  • Elevated Leucine is Neurotoxic
  • Sweet Urine odor
  • Tx: is dietary restriction
  • DIfferential (LOOK THESE UP)
    • PKU
    • Homocystinuria
    • Galactosemia
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123
Q

Tibial Bone pain. Lumpy protuberance over the right tibia + progressive hearing impairment for the last year. Bone biopsy shows Multinucleated cells, some containing over 100 nuclei.

What is the disease and what else can you tell me about its pathogenesis?

What is this multinucleated cell? What induces its differentiation into that cell type? what inhibits it?

A

Pagets DIsease of Bone (read in picture)

Osteoclasts

  • Is a monocyte subtype; The two most important factors for osteoclastic differentiation are
    • M-CSF
    • Receptor for Activated Nuclear factor Kappa-B (RANK-L)
    • Osteoprotegerin is a physiologic decoy recpetor that decreased RANK-L binding –> decreased osteoclast survival
  • FGF (chondrogenesis), IGF-1, TGF beta all favor bone deposition
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124
Q
A
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125
Q

Recurrent palpitations that start and stop abruptly. There is an abnormal conduction pathway in this patients heart beat that bypasses the AV node. What part of the ECG is most effected? What is the name for this process?

A
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126
Q

Young kid notices Dark Red blood on toilet paper. No Abdominal Pain. Low Hg. Tc pertechnetate scintigraphy –> RLQ.

A

Meckel Diverticulum

  • Ileal outgrowth results from failed obliteration of the vitelline (omphalomesenteric) duct
  • Painless GI bleed,
  • Can be a lead point to intussuception (currant jelly sttol)
  • TC pertechnatate scan has high affinity for parietal cells
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127
Q

What is the Clozapine used to Treat? What is the main side effect associated with this?

A

Treatment Resistant Schizporeia (associated w suicidality)

Main adverse effects in order: Agranulocytosis, Seizures, Myocarditis, Metabolic Syndrome

This second generation antipsychotic requires mointoring of absolute neutrophil count

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128
Q

GO OVER PSYCH DEFENSE MECHANISMS

A
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129
Q

Glucagon is upregulated in the fasting state an has its primary effect on what organs?

Epinephrine has its primary affect on what organs?

A

Liver

Epi = SKM, adipose tissue and renal cortex

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130
Q

What is the causes the earliest morphologic change in superficial thermal burn?

Deeper burn wounds form blisters due to what MOA?

A

Release of preformed histmaine from mast cells

Due to fluid extravasation through gaps b/n damaged venule endothelial cells

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131
Q

3 month onset of Heavy Menstrual Bleeding. Dysmenorrhea (pain). Uniformly Enlarged Uterus. Negative Urine hCH. No bleeding problems before. No pain with sex. What is the likely diagnosis? What are other findings/diagnostic criteria?

A

Adenomyosis

  • Endometrial glandular tissue within the myometrium
  • Normal appearing endometrial tissue on biopsy
  • Only diagnosed by microscopic exam of hysterectomy
  • DIfferential (ruled out)
    • Leiyomyoma (irregularly enlarged uterus)
    • Ectopic pregnancy (- hCG)
    • vWF disease (heavy menstrual bleeding had recent onset)
    • Endometrial hyperplasia (irregular, not painful)
    • Endometrial polyps (no uterine enlargement)
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132
Q

What does Blotchy Red muscle fibers on Gomori Trichome stain indicate? What is the inheritance pattern?

A

Mitochondrial myopathies

What are the 3 mitochondrial myopathies? (Look up)

  • which one is characterized by myoclonic epilepsy ?
  • blindess?
  • Stroke like episodes and lactic acidosis?
133
Q

LOOK UP QUESTION 5 in 5/27/20 practice test

A
134
Q

Family History of unexplained death. Echocardiography findings as follow: Overal increase in LV mass, Reduced LV cavity size, Assymetric increase in LV wall thickness (marked in crease in septum size ), Normal/increase LV ejection fraction, Left Atria enlargement. What is the likely diagnosis? What is the inheritance pattern?

A

Hypertrophic Cardiomyopathy(HCM)

  • Cause of Sudden cardiac death; often asymptomatic
  • Autosomal Dominant
  • Impaired diastolic function
  • Another characteristic finding is poorly developed coronary capillary network (in hypertrophied region) –> with evidence of ischemia (fibrosis, scarring)
  • Microscopiccaly shows myocyte disarray
    • Myosin heavy chain (sarcomeric protein) mutation
  • Harsh systolic ejection murmur
  • Differential
    • Cardiac adaption in athletes
      • eccentric hypertrophy with enlarged LV cavity
      • Uniform LV wall thickness increase (not just septum)
        *
135
Q
  1. The Locus Ceruleus is located where? What does it produce? What is the function of the Locus ceruleus? What pathology is caused by its abnormal activation?
  2. The Raphe Nucleus is Located where? What does it produce?
  3. What structures make dopamine? Where is it located
A
  1. Posterior rostral pons near the lateral floor of the fourth ventricle, NorEpenephrine. Arousal(reticular activating system), sleep-wake states, cognition, mood, blood pressure control (autonomics).Anxiety Disorders
  2. Medulla (serotonin)
  3. Ventral tegmental area & substantia nigra pars compacta. 3 Major pathways: Mesolimbic/mesocorticol (cognition + behavior), Nigrostriatal (voluntary Movement), Tuberoinfundibular (inhbit prolactin)
136
Q

Unresponsive patient, history of poorly controlled HTN (240/120 now), Extensor posturing + pinpoint pupils, CT scan shows acute pontine hemorrhage w mass effect. Autopsy shows disruption of all pigmented neurons in posterior rostral pons at the alteral floor of 4th ventricle.

These neurons produce what? What structure are they part of?

A

NE, Locus ceruleus

137
Q
  1. HMG-CoA reductase is the rate limiting step in __________. This enzyme is also a target of statin therapy.
  2. Cholesterol 7alpha hydroxylase is rate limiting step in ________. This is inhibited as a side effect of what medication?
A

Formation of Cholestorol Gallstones

  • 3 key MOAs involved in pathogenesis are
    • Increased Cholestorol
      • ex) Upregulation of HMG-coA reductase (Estrogen)
    • Decreased Bile Acids
      • ex)2. Bile acid synthesis, Fibrate medications
    • Decreased phosphatidylcholine
  • These will all lead to Bile becoming supersaturated with cholestorol –> precpitates into insoluble crystals
  • Risk factors
    • Obesity, rapid weight loss, female sex, glucose intolerance, hypomotility of GB (pregnant, long fasts)
138
Q
  1. Patient feels as sense of heightened arousal/ tension that quickly escalates to rage and uncontrollable impulses to be verbally or physically aggressive. Outbursts present relief that is usually followed by remorse. Describes what disorder? Treat with SSRI + CBT
  2. Frequent verbal or physical outbursts. Persistent irritability or anger between episodes. Child less than age 10. Described what disorder?
A

Intermittent explosive disorder (IED)

Disruptive mood dysregulation disorder

139
Q

What Drug is used to treat ADHD? What are there common adverse effects?

Lamotrigine is what type of drug and what is it used for? What is the key adverse effect>

A

Psychostimulants (methylphenidate and amphetamines)

Decreased appetite, weight loss and insomnia (less common are tics and inc HR/BP)

Anticonvulsant used to treat seizure + bipolar disorder –> Steven Johnson Syndrome

140
Q

Somnolence, decrease RR after ingesting 6 unknown pills. Improvement of RR w naloxone. what did he ingest?

what would be additional findings?

A

opiod intoxication

miosis. decrease bowel sounds, hypotension, dec tidal volume

141
Q

What is the likely are the 3 causes of a baby that presents at birth with a flat nose, club feet and signs of respiratory distress?

A
  1. Bilateral Renal Agenesis
  2. Posterior Uretheral Valves
  3. AR PKD
142
Q

What are the well known Hypercoagulable states include?

(8 of them)

A
  1. Post-Operative
  2. Malignancy
  3. Pregnancy
  4. Elevated homocysteine
  5. Nephrotic syndrome (loss of AT3)
  6. Smoking
  7. Inherited Thrombophilia (Factpr 5 Leiden, Prothromen Gene mutation, Antithrombin 3 deficient, Protein C/S deficient
  8. Antiphosholipid Ab syndrome
143
Q

Young kid with myocardial infarction, ocular lens displacement and intelectual disability.

  1. These Symptoms are a result of a build up of what substances?
  2. What is the Treatment?
  3. What Enzyme is most likely deficient?
A

Homocystinuria

  1. Build up homocysteine –> leads to methionine build up
  2. Cysteine supplementation is essential & limit methionine
  3. Cystathionine B synthase deficiency

Notes: Homocysteine is prothrombotic

144
Q

Defense Mechanisms Immature:

  1. Attributing one’s own feelings to others
  2. Transforming unacceptable feelings/impulses into the opposite
  3. Reverting to earlier developmental stage
  4. Avoiding conflict by expressing hostility covertly
A
145
Q

Extertional Heat stroke leading to Low platelets, Increased PT & aPTT are indicative of what ?

What other key Lab findings associated with this?

A

Disseminated Intravascular Coagulation

Elevated D-dimer (indicated Increased Fibrinolysis)

Low Fibronogen

Elevated thrombin

KEY diff: from HUS/TTP is the pt/ptt levels (normal in HUS)

146
Q

You have a malnourished patient come in. He is given thiamine, folic acid, multivitamins + IV dextrose. A few hours later the patient has significant muscle weakness. Serum phosphate is extremely low. What is the explanation for this response?

What are other causes of hypophosphatemia (differential)?

A

This is due to REFEEDING SYNDROME (search it up)

If you give glucose too fast then it will increase insulin –> redistributes Pi into muscle and hepatic cells because they require ATP for glycosis –> leads to even more decrease of Pi.

This can lead to cardiac (CHF) and respiratory failure

Key is refeed glucose back slowly so body can adjust.

147
Q

Right Leg injury. Pain in lower leg and cant bear weight. Tibial and fibular shaft fracture on Xray. Patient undergoes surgery + immobilization. Hours later he has severe pain in right leg. PE shows increased tension within anterior compartment. Which structure is most likely compromised?

What is in the lateral compartment? Deep posterior compartment?

A

Acute compartment Syndrome

  • Causes: long bone fracture, crush or thermal injury, bleeding disorders
  • Pressure in a compartment increased –> leads to vascular compromise –> severe pain and tissue ischemia
  • Most common locationL Anterior compartment of leg
    • Foot extensor muscle
    • Anterior tibial Artery
    • Deep peroneal Nerve
  • Lateral compartment
    • Superficial peroneal nerve (foot drop + sensation loss over foot) + proximal deep peroneal N.
  • Deep Posterior compartment
    • Posterior Tibial A, Peroneal A
    • Tibial N.
    • Decreased senation over plantar foot
148
Q

Blotting technique –> Substance detected –> Probe type

  1. Northern Blot –> ___________ –> ________
  2. Southern Blot –> ___________ —> ____________
  3. Western Blot –> ___________ —–> ____________
  4. Southwestern Blot –> ________ —> _______________
A

ELISA vs Western blot

  • ELISA = pt serum directly tested
  • Western proteins are first seperated by electrophoresis

SNOW DRIP

149
Q

Two most common enzyme mutation/defects in SCID?

A
150
Q

Isotype switching of B cells occurs in what section of the Lymph node? What cell signals are required for this?

A
151
Q

Look UP false negatives with sensitivity and specificiity

A
152
Q

Older child with cyanotic spells that improve with squatting, harsh systolic murmur + RV impulse is indicative of what?

What is the main cause of this disease?

What factor determines the severity of this disease?

A

Tetralogy of Fallot

  • Deviation of the infundibular septum –> causes all 4 problems
  • Severity of cyanosis/shunt is determined by degree of of subpulmonic stenosis
153
Q

Kartagener syndrome is due to a defect in what? What is a clinical complication? What is the triad

A

Form of primary ciliary dyskinesia

  • Due to a defect in Dynein

Triad:

  1. Chronic sinusitis (mucocillary defect)
  2. Bronchiectasis (recurrent resp infections)
  3. Situs inversus (organs on wrong side: organ migration)
  4. Also Infertility (flagella)
154
Q

2 month old infant. Progressive Hypotonia. Immigrant. Lethargy. Constipation. Large fontanelle, Large tongue, Umbilical hernia. What is diagnosis?

A
155
Q

When is a two sample t test used?

When is a chi-square test used?

When is a correlation coefficent used?

When is a meta analaysis used?

A
156
Q

Common Cancer Immunotherapy involve targetting two receptors that allow neoplastic cells to evade cellular immunity. What are these two receptors? (Melanoma & RCC)

Another type of immunotherapy induces ischemia and tumor necrosis via what mechanism? what is the name of this drug?

A

Anti-PD-1 Abs and anti-CTLA-4 Abs

157
Q

What is the genetic cause of Turner Syndrome? What gene winds up missing?

A

Most common: Meiotic nondisjunction during gametogenesis (45, X)

SHOX gene

Side note: Uniparent disomy is Prader willi/agenlman

158
Q

Non-fusion of the urethral folds is NORMAL process in what gender? What does it cause in the other gender?

A

Weeks 8-15: External genitalia

Normal in females –> Labia minora, vestibule of vagina

Failure of fusion in males –> hypospadias

side note: epispadias is associated with extrosphy of bladder and is caused by malpositioning of genital tubercle

159
Q

Explain the findings of the electrophoresis

A
  1. Hemoglobin A Will Travel the furthest/fastest because of its negative charge (glutamate)
  2. HbS (sickle cell) has valine (neutral AA) replace glutamate (negative) –> wont travel as far
  • Sickle cell trait has both HbS and HbA so thats why two marks
  • Sickle Cell disease has mostly HbS
  1. HbC has lysine(Postive AA) in the place of glutamate –> this results in even less migration
  • HbC Trait has both HbA and HbC
  • HbC disease has mostly just HbC
  1. Hemoglobin SC disease has HbS and HbC
160
Q

HbC and HbS both result from what type of mutation?

A

Missense

161
Q

Which Psych disorder is characterized by unstable and intense relationships. Mood reactivity, All or nothing ideation. Hard to control anger. Impulsive. Self mutliating behaivor.

A
162
Q

What is the first step of muscle contraction in terms of actin/myosin?

A
  1. Cell membrane depolarizes –> SR releases Ca2+ via Ryanodine receptor
  2. Calcium binds to troponin C on thin filaments –> conformational change and displacement of tropomyosin –> exposing myosn binding site on actin filament
  3. ATP is bound to myosin head –> cleaved to form ADP + pi (retained at head) –> myosin binds actin filament –> comfrmation change causes myosin to pull acin filament –> muscle contraction + ADP release
  4. New ATP is then bound to myosin head –> release of actin filament
163
Q

30 year female. bloody nipple discharge. No palpable masses or skin changes. No enlarged LNs. Otherwise healthy. What is the cause of this?

What is the histologic finding?

A

Intraductal papilloma

Proliferation of papilary cells in a duct or cyst wall with a fibrovascular core

164
Q

Most common cancers (excluding skin cancers) in women by incidence are? by mortality are?

A

Incidence: Breast, Lung, Colon

Death: Lung, Breast, colon

165
Q

Effects of Androgen Deprivation in Males:

Specifically decreases the ________ (not ____as much)

A

Specifically decrease prostate glandular volume (not stroma)

166
Q

A patient has Psychotic Symptoms (delusions/paranoia), Diaphoresis, tremors, tachycardia, HTN and mydriasis. These symptoms are most consistent with what?

A

Cocaine Intoxication

Must distinguish for PCP intoxication (Violent behavior + nystagmus)

167
Q

Middle age man. Hours of difficulty swallowing, dry mouth, and blurred vision. Major Depression History. Mydriasis and poorly reactive pupils. Normal nerve conduction velocity, but decrease compound muscle action potential. stimulating nerve helps. What is the like cause? and How does this condition happen?

A

Botulinum toxin from canned food

168
Q

Severe Neuropsychatric delay, >200 CGG trinucleotide repeats in chromosome X. What is the cause of this Disorder?

A

Fragile X syndrome

  • >200 repeats CGG trinucleotide repeats leads to hypermethylation of FMR1 (inactivation)
169
Q

What type of Hormones use receptors that contain Zinc fingers in their Motif?

What is the Signifcance of Zinc-fingers?

What type of hormones use second messengers?

A

Intracellular (lipid soluble) receptors contain Zing-fingers. Intracellular hormones include the steroid hormones(estrogen, aldosterone, cortisol), Thyroid Hormone and fat soluble vitamin receptors

Zinc-fingers –> are the most common DNA bind domain in humans (Many transcription factors use this). Intracellular receptors act as TFs.

Surface Receptors use Second messengers

170
Q

A cutip is inserted into the meatus in close contact withthe posterior wall. Patient suddenly becomes light headed and faint. He recovers with no problem. What nerve is irritated ?

A

Vagus Nerve –> Vasovagal syncope

Innervates posterior external auditory canal

171
Q

Hyperacute Rejection (Type 2 HS)

  • Onset: Minutes to hours ; Irreversible
  • characterized by preformed antibodies against graft HLA or blood group
  • Results in: fibrinoid necrosis and thrombotic occlusions of capillaries (cyanotic and mottled)
  • Antibody and complement mediated vascular injury + subsequent thrombotic occlusion

Acute Rejection (Type 4 HS)

  • Onset: less than 6 months; Reversible w immunsuppress
  • Cell mediated response (T cells)
  • Cell mediated: Lymphocytic intersitial infiltrate
  • Humoral: C4d deposition + Neutrophils & necrotizing vasculitis

Chronic Rejection

  • Months to years
  • Humoral
  • Vascular wall thickening + luminal narrowing
  • Intersitial fibrosis & parenchymal atrophy
A
172
Q

Sarcomere is defined as?

Where are actin(thin) filaments bound to structural proteins? How about myosin(thick) filaments?

What is the A band? Does it change length in contraction?

What is the I band? Does it change in length?

What is the H band? Does it change in Length?

A
  1. Sarcomere = Distance between Z lines
  2. Actin is bound to Z line; Myosin is bound to M line
  3. A band = ALL myosin (overlapped w actin and not); DOES NOT change in lengeth
  4. I band = region which actin does not overlap with myosin.

H band is region in which myosin does not overlap actin

BOTH get shorter in contraction

173
Q

What is the best method for determining whether a gene is undergoing transcription (due to a mutation in a non-coding sequence)? (ELISA, or one of the 4 blots)

A

You need to analyze for the presence of mRNA using NORTHERN blot. Better for assesing degree of transcription (Non coding = promoter or silencer)

174
Q

During the process of T cell maturation, TCRs demonstate very high affinity interaction with MHC molecules expressed on thymic medullary epithelial cells and dendritic cells. What is this process called?

What process occurs before this in the thymic cortex?

A

Negative selection

Positve selection

175
Q

Infant presents with signficant drooling, choking, coughing and cyanosis with feeding? What embryologic process went wrong? What are other associations?

A

Tracheesophageal fistula with esophageal atresia

  • Failure of lung bud to seperate from the primitive foregut
  • Polyhydramnios may be seen prenatally.
  • Inability to swallow saliva, food
  • X-ray will show stomach bubble (air flow )
176
Q

Look up Number needed to harm calculation

A
177
Q

During Total thyroidectomy a nerve is injured while ligating an artery that enters into the superior pole of the thyroid lobe. Which Nerve is it and which muscle will be denervated as a result of this injury?

A
  • Superior Thyroid Artery
  • External branch of Superior Laryngeal Nerve.
  • Crycothyroid Muscle (Only muscle innervated by this)
    • Acts to tense the vocal cords (injury = low hoarse voice)

The remaining laryngeal muscles are innervating by recurrent laryngeal nerves (Posteriorly: inferior thyroid artery)

  • Aryepiglotticus, lateral & posterior cricoarytenoid, thyroarytenoid muscles
178
Q

Fasting/Starvation

  • During the first _____ hours of fasting __________ is the main source of glucose
    • What are the Key steps in this Process?
  • After ______ hours, _______ is the main process used by body to maintain glucose level.
  • What are the key steps and enzymes of this process?
A

12-18 hours. glycogenolysis, formation of glucose-1 phoshpate

Gluconeogenesis

  • Glucose is formed from lactate, glycerol, glucogenic AAs
  • Goal is to bypass steps of glycolysis (Hexokinase, PFKinase, Pyruvate Kinase)
  • (1) Commited Step: Pyruvate –> Oxaloacetate
    • Via Pyruvate Carboxylase (requires <strong>Biotin</strong>; in mitochondria)
    • ​Then malate shuttle and back to OAA in cytosol
  • (2) Oxaloacetate –> PEP
    • via PEPCK
    • Both steps bypass pyruvate kinase
  • (3)Fructose 1,6 biphosphatase (bypass PFKinase)
  • (4)Glucose-6-phosphatase (Bypass Hexokinase)
179
Q

T2DM morpholohy?

T1DM morphology?

A

T2DM: amyloid deposition on pancreatic islet

T1DM: Pancreatic islet infilration with leukocytes (insulitis) & Abs against ilset antigens

180
Q

Digeorge Syndrome results in impaired development of which embryonic structures?

A

Impaired NCC migration into 3rd and 4th pharyngeal pouch.

181
Q

Patient with hypothyroidism –> what is the underlying Mechanism behind elevated LDL cholestorol in this pt? What is the Mechanism of elevated triglycerides?

A

Decreased LDL receptor Gene expression –> decreased clearance of LDL

Hypertryglyceridemia can occur due to decreased expression of lipoprotein lipase.

READ highlights

182
Q

Why does D-Glucose transport across plasma membrane of adipocytes and muscle tissue becomes much faster in the presence of insulin? What is this due to?

A

GLUT4 is the insulin sensitive transporter. It is stored in cytoplasmic vesicles. Increased number of these transporters = faster glucose uptake by the process of faciliated diffusion

GLUT2 facilitates export of glucose from liver, Small intestine & kidneys into the circulation

183
Q

MEN1 = Diamond or 3 Ps

  • What is the main feature?
  • Primary HyperPTH (hyperplasia or adenoma)
  • Pancreatic tumor (Gastrinoma)

MEN2A = Rectangle with star in middle

  • What is the main feature?
  • Pheochromacytoma
  • Primary hyper PTH (hyperplasia)

MEN2B: Ms + triangle

  • Medullary Thyroid Carcinoma
  • Pheochromacytoma
  • Marfanoid habitus
  • Mucosal neuromas
A
184
Q

A patient with HTN is being treated with a drug. He has Normal Na+, K+, BUN and Cr. Calcium is elevated and PTH is decreased. What is the cause of these lab values?

A

Thiazide Diuretic

185
Q

What substrate stimulates the first enzyme involved in a fasting state of 24 hours?

A

Commited step in gluconeogenesis is pyruvate carboxylase and is stimulated by acetyl coA

Citrate is + regulator of Acetyl coA carboxylase (FA synthesis) & F 2,6 Bpase (gluconeogenesis)

186
Q

Mortality reduction: single most biggest factor is?

A

Smoking cessation (especially in diabetes)

187
Q

GPCR proteins that contains alpha-helical regions composed of Valine, alanine and isoleucine perform what function in the cell?

A

Anchoring to Cell Membrane

188
Q
A
189
Q

The probability that a child from 2 populations with differant mutant allele carrier frequiencies will inherit an autosomal recessive disorder is 25% x CarrierFrequencyOne% x CarrierFrequencyTwo%

A

Example is Mom (1/30) and Father is 1/100)

1/30 X 1/100 X 1/4 = 1/12000

190
Q

A patient with poor sleep, feeling tired all day, snores loudl during sleep and frequently gasps for breath. BMI 30 + HTN. He has a bulky tongue and crowded narrow oropharnyx. What is the diagnosis? Stimulation of which nerve would help?

A

Obstructive Sleep Apnea, Hypoglossal N

191
Q

Severe shortness of breathe no tobacco use. Autopsy shows hyperinflated lungs, airway mucus plugging and cellular infiltration of the bronchial wall. What is this describing and what long treatment could have prevented this?

A

Uncontrolled asthma and Fluticasone

192
Q

A 60 yo patient. SOB. Dyspnea while lying flat and sleeping up right. JVD is present. Dullness to percussion at bialteral lung bases. Chest Xray shows cardiomegaly + bilateral effsuions. Serum protein is 6, and LDH is 60. What is the description of the pleural fluid and what be considered normal values of protein, LDH, glucose and WBC in the fluid?

A

Patient has heart failure –> transudative effusion

Light criteria

Exudative = increased capillary permeability so everything leaks out

Transudative = low pleural fluid/serum ratio

193
Q

Which asthma med works by inhibiting the interaction of inflammatory mediators with sell surface receptors (reduce bronchoconstriction)?

Which Asthma med works by inhibiting NFkB –> anti-inflammation. Also inhibits phospholipase A2?

Which Asthma med inhibits the enzyme 5-lipoxygenase –> reduce production of LTs?

A
  1. Montelukast
  2. Inhaled ICS
  3. Zileuton
194
Q

What determines the total airway resistance in the Lower Respiratory Tract?

Where is airway resistance the highest?

A

Since the airways arrange in parallel, airway resistance in determined by the total cross-sectional area of all airways at the level. The greater the total cross sectional area –> the lower the airway resistance

Highest in medium sized bronchi

195
Q

Candida Albicans can cause lung infection?

A

NAAAA bitch

196
Q

Sputum cultures on selective medium appear as parallel chains (serpentine cords). This growth indicates what organism and what is the significance?

What are other components of this organism?

A

TB cord factor (virulence factor) –> prevent macrophage mediated desctruction and helps make caseating granuloma.

197
Q

What is the pathway of fetal circulation?

A

Placenta –> umbilical vein (most O2) –> ductus venosus –> Inferior Vena Cava (SVC not participate) –> R. Atrium (rest of heart via foramen ovale) –> pulmonary circulation –> ductus arterosis –> descending aorta –> paired umbical arteries –> placenta

198
Q

What is the major stimulator of respiration in healthy individuals? What is stimulated and where?

What changes to this process are seen in COPD?

A

Healthy: Central Chemoreceptors locate in the medulla

  • Sense high CO2
    • Respond to hypercapnia (& H+) –> Inc RR

COPD: Peripheral chemoreceptors (carotid body:CN9 and aortic body:CN10)

  • Sense PaO2
    • stimulated by hypoxemia –> increase RR
    • inhibited by oxygen supplementation –> Dec RR
  • reponse to CO2 is blunted in COPD
199
Q

Silicosis key finding? What is a consquence of this and why?

A

TB infection due to impaired macrophage function

Classic finding would be egg shell calcification

200
Q

The Work of Breathing in Restrictive lung disease is chracterized by?

The work of breathing in Obstructive lung disease is characterized by?

A

Restrictive = rapid shallow breathing (low tidal volume)

Obstructive = low RR, slow deep breathing; (high tidal volume)

201
Q

Transpulmonary pressure vs Lung Volume Graph measures what?

A

Compliance

202
Q

Midline mass that moves superiorly with protrusion of tongue or swallowing. Can be infected after URI. What is the Dx? what other midline mass can you rule out?

What would be the likely Differential of a lateral neck mass?

A
  1. Thyroglossal duct cyst is the diagnosis. You can rule out dermoid cyst because those DO NOT move with swallowing
  2. Carotid body tumor, Cystic hygroma, Brachial cleft cyst
203
Q

Teenager with painless mass in right scrotum. Nodule felt on PE. Does not change in size with positioning and no transillumination. No LAD. What is diagnosis?

A

Painless, solid scrotal mass should be considered testicular cancer until proven otherwise.

204
Q

What are the two main types of genetic anomalies that give you down syndrome?

A

Meiotic non disjunction(47 XX +21) and Unbalanced Robertsonian translocations( 46 XX, t(14;21))

205
Q

Name the Congenital Defect:

  1. Protruding tongue, excessive skin at nape of neck, upslanting palpebral fissures. VSD
  2. Low set ears, webbed neck, wide spaced nipples, coarctation of aorta
  3. Hypertelorism, micrognathia, cleft palate, ToF
  4. Micrognathia, low set ears, clenched hands with overlapping fingers, hypertonia
  5. Microopthalmia, cleft lip and palate, polydactyl. holoprosecnphaly
A
  1. Down Syndrome
  2. Turner Syndrome
  3. DiGeorge
  4. Edward
  5. Patau
206
Q

What Specific Defect leads to recurrent Neisseria infections?

What problem can lead to severe Neisseria infection?

A

Deficiency of membrane attack complex (factors C5b -C9)

TOO MUCH IgA (all it does is bind to bacteria and prevents attachment to mucosal surfaces). This will prevent IgG or IgM from binding leading to less activation of complement and clearance of bacteria

207
Q

UWORLD look up how to calculate false positive and negative

A
208
Q

What functions are the frontal lobes responsible for?

What area/lobe is responsible for language comprehension?

Lesions in what lobe would give you right-left disorientation and finger agnosia?

Lesions that result in inability to recognize a familiar face?

A

Personality, Language, motor functions and execute functions(abstraction, planning, inhibition, attention and working memory)

209
Q

Peptic Ulcers(stomach or duodenal mucosa) are most commonly due to what?

A

H. Pylori and NSAIDs

What is the MOA of NSAIDS and its effect gastric mucosa? (dont open picture till you answer)

210
Q

Young female, normal BMI. Gestational diabetes and fasting hyperglycemia are genetically predisposed. What enzyme is likely reduced in activity?

What is the mechanism of Insulin relase by pancreatic beta cells? What stimulates it?

A

Glucokinase

Stimulated by glucose + AA

Inhibited by epinephrine

211
Q

LOOK UP INFORMED CONSENT

A
212
Q
  1. What is the pathogenesis behind migraines? What pharm therapy targets this?
  2. What is the pathogenesis behind absence seizures?
  3. What is the pathogenesis behind narcolepsy?
A
  1. Increased cerebral excitability –> wave of cortical spreading depression –> release of calcitonin gene-related peptide (vasoactive) by trigenminal afferents –> pain transmission. Triptans and Erenumab
  2. Dysfunction of thalamocortical fiber Ca2+ channels
  3. Orexin A and B (hypothalamus) –> inhibit transition to REM sleep
213
Q

What is the MOA behind Renal Changes during pregnancy? What does this due to the following:

GFR

RBF

Serum Creatinine

Cardiac Output?

A
214
Q

___________ (in series) –> group 1b –> sense Tension (not length) –> too much force results in sudden muscle relaxation (prevent damage: negative feedback)

_________ (parallel) –> Group 1a & 2–> sensitive to change in muscle length –> Mediate stretch (myotatic reflex; DTRs) ; contraction that resists stretch

A
215
Q

What is the MOA of latanoporst in glaucoma?

What is the MOA of dorzolamide?

What is the MOA of Timolol?

What is the MOA of Brimonidine?

What is the MOA of muscarinic agonist?

A
216
Q

What viral infection are patients that undergo transplant and immunosuppression susceptible to reactivate? What are the manifestations? What is first line therapy for this and associated side effects?

A
217
Q

STEMI treatment. What was the TX responsible for the rapid reperfusion?

What is the drug used in Treatment + prevention of Venous thromboembolism?

What is the Treatment used to treat heparin-induced thrombocytopenia?

What two drugs are irreversible inhibitors of platelet aggregation? used in STEMI regimen?

How does Heparin work?

A

Alteplase

218
Q

Teenager with 1 day of left testicular pain. Pain is worse with movement. Swelling and TTP on posterior and superior Testis. Other testis is normal. Cremasteric reflex is normal. Urinalysis has numerous leukocytes w no bacteria. What is Dx and what is the cause?

A

Acute epididymitis

219
Q

LOOK UP VOLUME OF DISTRIBUTION FOR PHARM

A
220
Q

Urine turns black overnight + Arthritis with black pigment in cartilage. What is Diagnosis? What Enzyme is deficient? What conversion process is affected?

A

Alkaptonuria

  • Autosomal Recessive (Tyrosine metabolism)
  • Deficiency of homogentisic acid dioxygenase
  • Conversion of Tyrosine –> Fumarate
  • Retained homogentisic acid binds to collagen in Connective tissue, tendons and cartialge
  • Symptoms:
    • Black Urine overnight (Oxidation)
    • Onchronosis
      • Blue black pigment (ears, nose, cheeks)
    • Onchronotic arthropathy
      • Black pigment in cartialge joints
221
Q

Gap Junctions are made of what type of protein? What is the Function?

Tight junctions?

Adherens Junctions?

Desmosomes?

Hemidesmosomes?

A
222
Q

What medications can you do to approximate physiologic insulin secretion?

A
223
Q

Older pt. Admitted to hospital for increasing LE edema and dyspnea. History of Pulm HTN, obesity hypoventilation syndrome and chronic LE edema. What is his likely diagnosis at this time?

5 days after admission his Hg, BUN, and Cr all go up alot. Elevated BUN/Cr ratio. Low Urine sodium. What is the likely cause for these abnormalities?

A
224
Q

Patient SOB is worse with lying flat, dyspnea, bilateral basilar crackeles and S3 heart sound. Decrease Pulse Ox. High RR. What is diagnosis?

These findings suggest pulmonary edema, how does this present in terms of lung function, compliance?

A
225
Q

What are the symptoms of opioid withdrawal and what other drug can precipitate withdrawl and how?

A

Buprenorphine (partial agonst)

226
Q
A
227
Q

What is the treatment for tonic-clonic seizures mixed with absence seizure episodes?

What about absence seizure alone?

How about focal seizures?

A
228
Q

Apical holosytolic murmur months after an MI. Resolves with diuretic and vasodilator Tx. What is the murmur and what is the likelt cause?

A

Mitral Regurgitation secondary to decompensated heart failure

229
Q

Which Nerve is injured deep to the mucosa of the overlying piriform recess?

A
230
Q

Hematuria, flank pain, 3+ blood in urine. Compression of Left Renal vein between the SMA and aorta. What is Dx and complication?

A

Varicocele (nutcracker syndrome) due to pressure elevation and retro grade flow

231
Q

30 yo female with severe joint pain in hands, wrist and ankles for a week. Unable to perform daily activities. High fever and and diffuse rash during a trip to Puerto Rico 2 weeks ago. No other red flags. Periarticular swelling + tenderness of said joints. Decreased ROM. Lymphopenia. What is cause of joint pain?

A

Chikungunya fever, alpha virus

232
Q

34 yo Female. Mass in breast. 2cm nodule. What is Dx?

A

Fibroadenoma

  • Most common benign tumor of breast (young women15-35)
  • Well demarcated painless mobile
  • myxoid stroma that encircles epithelium-lined glandular and cystic spaces.
233
Q

3 week old infant. Lethargy and difficult to arouse. Did not recieve any vaccinations or medications after birth. Head circumference is 99th percetile. Weight and length are 25th. Large, bulging anterior fontanel. Eyes appear driven downward and cant move up. Intracranial hemorrhage is seen on CT. What is the cause?

A

Vitamin K deficiency –> impaired clotting factor carboxylation

234
Q

What are the Risk factors for Uric acid Kidney stones? What is the treatment?

A
235
Q
A
236
Q

5 day old infant. Multiple vomitting spells. Tachypnea, hypotension. Jaundice, lethargy, sunken fontanelle, dry mucous membranes, hepatomegaly. Hypoglycemia + ALT elevation. Normal ammonia. Gram negative rods. Infant placed on special formula and improves. What is the disorder and what enzyme is deficient?

A
237
Q

What is the general rule for lymphatic drainage of Large intestine?

Where does Lymph drainage proximal to anal dentate line go to (what major LNs?

How about distal to the anal dentate line?

A
238
Q

Sharp and pleuritic chest pain that is exacerbated by swallowing and coughing. Diffuse ST elevations. Happens 3 days post MI. What is the cause?

What if it was a week to a month out?

A

Pericardial inflammation over the overling necrotic segment (peri-infarction) pericarditis (follows a transmural MI)

Pericardial inflammation due to autoimmune reaction to necrotic tissue (dressler syndrome)

239
Q

What is the difference between Postpartum blues, postpartum depression and post partum psychosis?

A
240
Q

What medication impairs the cell-mediated immune response and leaves people susceptible to intracellular bacteria and granulomatous fungi?

A

TNF-alpha inhibitor

241
Q

What are the steps of Insulin receptor cell signaling propogation?

What subtances inhibit or cause insulin resistance and how?

A

STep1: Insulin binds

Step2: Activate Tyrosine phosphorylation (autophosphyrylation)

Step 3: Binding of substrates (IRS-1/2) –> downstream effect

Step4: PIK3 –> GLUT4, glycogen, lipid, protein synthesis

MAPK: cell growth and DNA sytnehsis

TNFalpha, Glucagon, epinephrine, glucocorticoids (phosphorylation of threonine or serine residues on IRS)

242
Q

Lactose fermenting, indole postive gram negativ rod?

A

E. Coli

243
Q

Most Rodentacides contain what? (Hint: symptoms are bloody emesis, scattered ecchymoses, blood in stool)

What is the treatment for this?

A
244
Q
  1. Which Drug is indicated in insanely high Triglyceride levels?
  2. Which drug is used for prevention of CV disease and major use is lowing LDL cholestorol?
  3. Which two drugs are used in hypercholesterolemia?
  4. Which drug increased HDL, but has alot of side effects like flushing?
A
245
Q

What is the MOA of antiobiotic that is used to treat enterococcus and side effect is tinnitus/hearing loss + renal issues?

Which Abx worls by creating transmembrane channels tha cause ion leakage and cell membrane depolarization? what are its side effects?

A

AMinoglycosides inhibit genetic code reading and protein synthesis by binding to prokaryotic 30s subunit.

246
Q

Which metalloprotease breaks down polypeptides released for the heart that are responsible for vasodilation, diuresis and inhibition of RAAS?

A

Neprylisin

247
Q

Hematogenous osteomyelitis in kids effects what bone region?

A
248
Q

2 yo girl ambigous gentialia, Clitoral enlargement. High blood pressure. Hypokalemia. What enzyme deficient?

2 week old girl ambigous genitalia, hypotension, hyperkalemia, N/V. What enzyme is deficient?

2yo boy with ambigous gentialia. Hypertesion and hypokalemia. Often diagnosed at puberty?

A
  1. 11-beta hydroxylase deficiency (HTN due to weak mineralacorticoid build up (acts like aldosterone)
249
Q

Which drug is used as an anticonvulsant and mood stabilizer? Can effectively treat Bipolar disorder + epilepsy. What are this medications side effects?

What are other mood stabilizers used in Bipolar disorder?

A

Valproate

Tell me key side effects?

250
Q

Describe MOA of acute viral hepatits and morphology of acute vs chronic

A
251
Q

What is the typical stool finding in watery diarrhea? Specifically Vibrio?

What is the typical stool finding in bloody diarrhe?

How about diarrhea caused by Typhoid Fever?

A
252
Q

What are the symptoms of Serotonin Syndrome? What is the most important one?

What are common medications that can cause it?

A
253
Q

Some MRSA carry a cytotoxin that destorys leukocytes and causes tissue necrosis what is this called?

What is the main virulence factor of Strep Pneumo?

A
254
Q

Severe Dry eyes and Dry mouth are characteristic of what disease?

What are the Serologic Markers for this?

What is the site of biopsy? What is seen on histology?

A

Sjogren’s Syndrome

Anti-Ro (SSA) and anti-La (SSB)

Lip biopsy (periductal lymphocytic infiltrates)

255
Q
A
256
Q

Explain the mechanism of acute kidney injury by NSAIDS. What part is effected?

A

Prostaglandins cause vasodilation of the afferent arteriole leading to increased GFR and RBF. NSAIDS inhbit PG production –> block vasodilatory effects. (pre-renal azotemia)

What medication causes efferent arteriole vasodilation (lower GFR) ?

257
Q
A
258
Q

Omeprazole blocks what channel?

Tedrodotoxin & Lidocaine block what channels?

Verapamil blocks what channel?

Dofeltilide blocks what channel?

A
259
Q

Look up relative risk reduction

A
260
Q

Look up Cutoffs

A
261
Q

All patients with a major depressive episode should be screened for ___________ before Treatment. Why?

A

Past history of manic episode (Bipolar disorder) antidepressant monotherapy can carry a risk of inducing mania.

Not as important as first part: history of sexual dysfunction may be of concern to some people

262
Q

What part of the colon is always involved in Hirshprung’s disease and what is the mechanism/reasoning behind this?

A

Rectum

(NCC cells move caudally along vagal N; proxmal colon at 8th week and rectum by 12th week) if disruption in this process rectum will always be involved

263
Q

Phenylketonuria can be caused by a 1. deficiency in phenylalanine hydroxylase OR 2.deficiency of __________________ which forms _______ (a cofactor used in the synthesis of ________, ________, _______. What is the treatment of this second form.

Both causes lead to excess Phenylalanine.

A

Dihydrobiopterin reductase, BH4 –> Tyrosine, Serotonin and DOPA (precursor to NE, E and D)

264
Q

Acute onset constipation. Lung carcinoma. Increasing low back pain. Dry cough. weight loss. increasing difficulty with urination. Pain over the lower spine. Bilateral LE weakness. Sensation impaired in perineal region. What is Dx? What is causing the constipation?

A
265
Q

What are the pulmonary changes seen with aging?

A
266
Q

What is the main mechanism of copper removal in healthy human body?

A

Hepatic secretion into bile and excreted in stool

267
Q

What is the finding on biopsy in a patient with lactate deficiency?

A

Normal Bowel mucosa

268
Q

What are the effect of opioids(morphine) on the spinal cord neurons (2)?

A
  1. Bind to Mu receptor(inhibitory G protein) –> closure of voltage gated Ca2+ channels –> reduce calcium influx –> decrease Excitatory NT release (presynaptic terminal)
  2. Bind to Mu receptor on postsynaptic terminal –>opens K+ channels ==> hyperpolarization (K+ efflux)

Lidocaine works by inhibiting voltage gated Na+ channels

269
Q

Teenager. Difficulty moving. Progressively worsening symptoms. Kyphoscoliosis, high plantar arch. Relative with neurologic issues + HF at age 25.

What is Diagnosis?

Can you explain the cause of his movement issues?

What gene?

A
270
Q

What is the best/most sensitive test to order when assesing patient with impaired nutrient absorption (loose stools)?

A

Sudan 3

271
Q

What AIDS defining illness would be seen with a CD4 count of less than 50? What are the symptoms?

A
272
Q

What part of the kidney is erythropoetin released by? In respose to what?

A

Peritubular (interstital cells) Fibroblasts in renal cortex

In response to decreased renal oxygen delivery

273
Q

How long does it take for vitamin B12 stores in the body to deplete? What are some known causes of B12 deficiency?

A
274
Q

Explain OCD

A
275
Q

In anti-epileptic drugs: blocking voltage gated Ca2+ channels. What subsequent step will not occur?

A

Fusion and release of NT from vesicles

276
Q

Progressive fever with, relative bradycardia, followed by salmon colored macules on the trunk and diarrhea describe what disease?

A

Typhoid Fever

277
Q

Influenza virus pt. Superinfection can happen by what 3 bacteria? What is the one that is likely to infect young, healthy patients?

A

Strep pneumoa, haemophlilus influenza, and Staph aureus

Staph aureus can cause it in younger previously healthy pts

278
Q

What is the mode of inheritance?

  1. CF, Hemochromatosis, Sickle cell
  2. Huntington, Marfan, MEN, NF
  3. Myoclonic epilepsy, MELAS & leber hereditary optic neuropathy
  4. Duchenne/Becker Muscular dystrophy, hemophilia, G6PD deficiency?
  5. Spina bifida, Cleft palate, HTN
A
  1. AR
  2. AD
  3. Mitochondrial
  4. X-linked Recessive
  5. Multifactoral
279
Q

Herpez Zoster (shingles) presents as what?

A
280
Q

Chronic Transplant rejection is characterized by what findings?

Acute Transplant rejection is characerized by what?

Hyperacute?

A
  1. Irreversible, obliterative vascular wall thickening with tubular atrophy and interstial fibrosis
  2. Dense, intersitial, mononuclear(lymphoctic) infiltrate; T cell medaited
  3. Vascular fibrinoid necrosis with capillar thrombotic occlusions
281
Q
A
282
Q

What are all the effects of Angiotensin 2?

A
  1. Efferent arteriole constriction –> Raise GFR, dec RPF
  2. Increased Na/H20 reabsorption
  • Proximal tubule via capillary effect
  • Direct proximal tubule resportion through Na/H+ exchange
  1. Aldosterone release
  2. Pituitary ADH secretion
  3. SNS activation
283
Q

What is CardioRenal Syndrome caused by?

What are the 3 Main Renal effects?

A
284
Q

pt with tonic/clonic seizure, headache, vomitting, confusion and Fever. Papilledema. Neck Rigidity. Patient died, Biopsy is seen

A

Yeast with thick polysaccharide capsule (cryptoccoccus neoformans)

285
Q

What medications are common cause of QT prolongation?

What are common causes of AV block?

A
286
Q

30 year old patient. Severe palpiations and light headedness. Has had similar epeiosdes in the past. SHe is asymptomatic 30 mins after arrival. Shows Delta waves. What is the cause?

A
287
Q

The same antiobiotic are given at two different dosages. One is every 6 hours(1 gram) and the other is every 12 hours(2 grams).

Which will have improved patient compliance? which will have lower average plasma drug level? Which will have lower drug toxicity?

A
288
Q

How does te foramen ovale close? what is a rare complications years later if it remains patent?

A
289
Q

Where is a likely sign for common fibular nerve injury?

What does the common fibular nerve branch into? What compartments do these supply? What areas of the foot? Which one does foot dorsiflexion vs eversion?

A
290
Q

What are the manifesations of Carcinoid tumor? What dictates when it becomes carcinoid syndrome? What is a longterm complication?What is the treatment?

A
291
Q

Pure Sensory stroke is most likely to becaused by a lesion in what location?

Pure Motor stroke would be a result of lesion where?

A lesion causing contralateral weakness and ataxia due to involvement of corticospinal and corticobulbar tract would be located where?

A lesion causing behavior issues (agitation, psychosis, abulia), speech/language issue and choreathetosis would be located where?

A
292
Q

Autopsy shows 5 to 6mm cavities in deep structures of the brain filled with clear fluid? what is the cause of these findings?

A
293
Q

What is clinical presentation of Infant botulism?

A
294
Q

A women gives has a stillbirtth at 20 weeks. A few weeks ago she had pain in both knees, and ankles that resolved in a week. She is a third grade teacher. Autopsy of fetus shows pleural effusion, pulmonary hypoplasia and ascites. What virus is the cause? Is it an RNA/DNA virus? ss or ds? Enveloped or not?

What are some other TORCH infections?

A

Parvovirus B19, enveloped, ssDNA

295
Q

What does the TORCH mnemonic stand for?

Which one causes limb hypoplasia, cutaenous scarring, cataracts, chorioretinitis?

Which one causes hydrops fetalis?

Which one causes chorioretinitis, intracranial calcifications, hydrocephalus?

Which one causes “snuffles”, hepatomegaly, skeletal anomalies?

Which one causes Sensorineural deafness, catarcts and blueberry muffin rash, HSM, heart defects?

Which one causes deafness, periventricular calcifications, jaundice, HSM, chorioretinits?

Which one causes Cutaneous vesicles, lesions, scarring?

A
296
Q

Why do PPIS need to be slowly tapered off?

A
297
Q

What are pneumoconiosis?

A
298
Q

Persistent, profuse mucoid diarrhea. Hypokalemia and microcytic anemia. 2,5 cm, cauliflower like mass in sigmoid colon. What is diagnosis?

A
299
Q

25 yo male normal male pattern facial and pubic hair. SMall testes and decreased sperm count. Normal testosterone. What is Dx?

A
300
Q

Which Key growth factors promote angiogenesis in neoplastic and granulation tissue?

Which cytokine are indirectly involved and can stimulate one of these growth factors?

A
301
Q

Hepatitis B vs Hepatitis C

Transmission?

Acute syndrome?

Symptoms?

Chronic State?

A
302
Q

What type of Immunoglobulins do blood group A or B mothers have circulating?

How about blood group AB?

How about blood group O?

A
303
Q

Diabetic Mononeuropathy can can cause diplopia, down and out eye, and ptosis by which mechanism?

How is this different from the other cause of mononeuropathy?

A
304
Q

Brain abscess appears as what on CT? and arise from what location in the body? what species?

What would cause a temporal lobe abscess?

A
305
Q

Older patient has 6 month Hx of chest tightness when he walks uphill or climb stairs. Radiates to his throat. Last 5- 10 minutes before going away. T2DM plus Increased LDL. Father had CABG & mom had stroke. What does he likely have?

What medication does the metabolite S-nitrosothiols come from? This drug effects vascular smooth muscle in which part of the body? Tx leads to relief of Symptoms.

A

Stable angina pectoris.

Relieved with nitrate (nitroglycerin. isosorbide mononitrate/dinitrate) –> metabolized to nitric oxide and s-nitrosothiolds.

Predominantly effects LARGE VEINS (venodilation) –> decrease preload (lower Myocardial O2 demand)

306
Q

How can you tell that a patient with mitral valve stenosis also has aortic valve involvement?

A
307
Q

CMV retinitis is the most common cause of eye disease in AIDS patients with CD count below 50. What will fundsocopy show? Treatment?

A

Yellow, white fluffy retinal lesions, near retinal vessels also has hemorrhage

Gangciclovir.

308
Q

Hyaline casts are made up of? Caused by?

Fatty casts are made up of? caused by?

Waxy casts are made up of? Caused by?

Granular (muddy brown) casts are made up of? caused by?

WBC casts are made up of? caused by?

RBC casts are made up of? caused by?

A
309
Q

What findings is most indicative of a poor prognosis of cirrhosis?

A

Tests of Liver function

  1. Elevated Prothrombin time
  2. Low albumin
  3. Elevated BR
310
Q

Look up correlation coefficient

A
311
Q

What is the mechanism of of the pictured lung condition in a 45 year smoker?

A
312
Q

Treatment of metastatic prostate cancer.

What does Leuprolide inhibit?

What does Ketoconazole, spironolactone inhbiit?

What does Finasteride inhbiit?

What does flutamide, spironolactone, cyproterone inhibit>

A
313
Q

Early fall season. 43 yo. 4 weeks of cough. Initially a bad cold and the other symptoms stopped but the cough has stayed and worsened. Bursts of coughing for minutes and unable to clear mucus. So heavy he vomitted after. teacher. all vaccinations recieved, but hasnt seen doc in years, nothing on chest xray. WHat is dx?

What are its main toxins

What is a unique lab feature?

A

Pertactin

Pertussin Toxin

Lymphocytosis

314
Q

Middle age women. Several “near collisions” driving at night. Generalized pruritis. Hasnt seen dr in years. Skin is diffusely course and dry. What could have caused this?

A

Pruritus due to Bile acid deposition

Hyperkeratosis + night due to Vit A deficiency

Cause of vit A deficiency are?

What is Dx?

315
Q

Patient has diabetes that requires insulin therapy. Hisotry of HTN, hyperlipidemia and migraines. In the morning her blood glucose is 42. She says she feels hungry but has no symptoms of hypoglycemia. What medication can explain her lack of hypoglycemic symptoms? What is the mechanism behind this?

A

Non selective Beta blockers (Propranalol)

Think about the MOA behind this.

In response to hypoglycemia the body activates ____________. This results in two distinct pathways that cause different array of symptoms. What are the different mediators of these two symptoms? What symptoms do they cause?

316
Q

Has a puncture leg wound. Right foot is dorsiflexed and everted. The patient cannot stand on his tip toes. No fractures, and pulses are intact. What nerve is damaged? Where would sensory loss be?

A
317
Q

A diabetic patient is experiencing recurrent hypoglycemic episodes (below 50 on multiple occasions). The patient has CKD from diabetic nephropathy. GFR has declined to 20. Why is he havving these symptoms?

A

Due to decreased insulin clearance by the kidney (exogenous insulin). Insulin clearance is dependent on GFR

NOT increased glucose excretion (this is hyperglycemia)

318
Q

Explain the different mechanisms of contraction between SKM, cardiac and smooth muscle.

Why does verapamil have minimal effect on SKM?

A
319
Q

Screening for early stage diabetic nephropathy is best accomplished by measuring urinary excretion of what?

What would be a good Tx that can reduce mortality if this subtance is increased in urine?

A

Albumin

ACE- inhibitors

320
Q

Punch biopsy of normal looking epidermis shows stellar cells with intracytoplasmic granules in shape of tennis racquet. These cells have myeloid surface markers and can interact with T cells. What is this cell type?

A
321
Q
A
322
Q
  1. Defective ApoE leads to elevated ______. manifests as _______, ______ and ______
  2. Defective __________ or ApoB-100. Lead to elevated ____. Manifests as ________, _____ and ____
  3. Defective _______ or ApoC-2. Leads to elevated _____. Maninfests as ________, ________
  4. ApoA1 and LCAT deficiency –> Low levels of ____ and increased _____
  5. Familial Hypertrycleridemia will have elevated levels of ____?
A
  1. VLDL and Chylomicons. Premature atherosclerosis
  2. LDL receptor. Premature atherosclerosis, tendinous xanthomas.
  3. Lipoprotein Lipase. Chylomicrons, Acute pancreatitis
  4. Low HDL and increased free cholestorol
  5. VLDL
323
Q

Teenager. Never menstruated. Fully developed secondary sexual characteristics. Shorted vaginal canal with rudimentary uterus? What is Dx?

A
324
Q

Severe respiratory distress. Patient needs intubation. Ketamine is given. What purpose does it serve for thisc scenario?

What two other medications are used and why?

A

Ketamine NMDA antagonist (similar to PCP); preserves respiratory drive. Also an anesthetic. Ketamine –> stimulate catecholamine reease (sympathomimemtic) –> bronchodilation

Propofol and Etomidate

NM blockade (succinycholine or rocuronium)

325
Q

You need to counsel diabetic patietns taking insulin about weight gain (dont ignore because it may lead to reduced adherence)

A
326
Q

Explain the mechanism behind Cystic Fibrosis. How is it caused?

A
327
Q

2 yo. Recurrent infections. Always sick. Otitis media, skin infections, pneumonia, Staph aureus on skin infection. DECREASED CD18 Antigens on surface of leukocytes. What is diagnosis? What is patient at risk for? What is CD18?

A
328
Q

What is persistent depressive dirosder?

A
329
Q
A