UWORLD random 3/17 Flashcards

1
Q

DM I sx

A

polyuria
polydipsia
polyphagia

fatigue
weight loss

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2
Q

delirium tx

A

haloperidol

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3
Q

lesions that cause ONLY inguinal LAD

A

medial LE

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4
Q

lesions that cause BOTH popliteal and inguinal LAD

A

lateral LE

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5
Q

Western Blot

A

protein

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6
Q

Southern Blot

A

DNA

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7
Q

Northern Blot

A

mRNA

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8
Q

Southwestern Blot

A

DNA-bound protein

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9
Q

CML genes

A

BCR-ABL fusion gene

t(9;22)

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10
Q

metabolism of v long fatty acid chains/branch chain at odd-numbered fatty acids

A

peroxisomes

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11
Q

Zellweger syndrome

A

peroxisomal disease

unable to form myelin in CNS

hypotonia, seizures, hepatomegaly, mental retardation, early death

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12
Q

refsum disease

A

peroxisomal disease

defect in a-oxidation

neuro disturbances from phytanic acid accumulation

tx = avoid chlorophyll

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13
Q

glossopharyngeal nerve

A

IX

stylopharyngeus muscle (elevate larynx during swallowing)

parotid gland secretion

sensory = tympanic membrane, eustachian tube, posterior third of tongue, tonsillar region, upper pharynx, carotid body/sinus

taste = posterior third of tongue

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14
Q

glossopharyngeal nerve lesions

A

loss of gag reflex

loss of sensation in upper pharynx, posterior tongue, tonsils, middle ear cavity

loss of taste in posterior 1/3 tongue

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15
Q

when b-hcg is detectable in serum

A

6-8 days after fertilization

implantation 6 days after fertilization, syncytiotrophoblast starts secreting b-HCG

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16
Q

when b-hcg is detectable in urine

A

14 days

17
Q

RA pressure

A

<5

18
Q

RV pressure

A

25/5

19
Q

Pulm artery pressure

A

25/10

20
Q

LA pressure

A

<12

capillary wedge

21
Q

LV pressure

A

130/10

22
Q

Aorta pressure

A

130/90

23
Q

PE acid/base disturbance

A

hypoxemia

respiratory alkalosis

24
Q

live attenuated oral poliovirus vaccine Sabin vs inactivated Salk

A

secretory IgA in intestinal lumen

25
Q

ischemia on CT

A

hypodense

poorly delineated from surrounding tissue

26
Q

post-ischemic brain injury timeline

A

48 h = red neurons

3-5 days = neutrophils
followed by monocytes

2 wks = cystic space replaces necrosis
gliosis (astrocytes form glial scar)

27
Q

lipids in microglia

A

phagocytosis of disintegrated neurons, myelin, necrotic debris

myelin breakdown products

28
Q

acute intermittent porphyria

A

AD

porphobilinogen deaminase deficiency (PBG –> HMB)

29
Q

AIP sx

A

mostly asx

acute attcks = abdominal pain, vomiting, peripheral neuropathy, neuropsycho sx, reddish-brown urine

30
Q

AIP tx

A

IV glucose or heme preps

downregulate ALA synthase activity (reduce toxic intermediate metabolites of heme synthesis)

avoid CYP450 inducers

31
Q

normal CD4+ lymphocyte count

A

> 500

32
Q

polymyositis sx

A

symmetrical prox muscle weakness

increased difficulty climbing stairs, getting up from chair, carrying heavy objects

33
Q

polymyositis pathology

A

+ muscle enzymes (CK, aldolase)

autoantibodies (ANA, anti-Jo-1)

MHC 1 antigens on sarcolemma with CD8+ cytotoxic T-cells, myocytes

34
Q

polymyositis biopsy

A

inflammation
necrosis
regeneration of muscle fibers

(patchy necrosis)

35
Q

Baclofen

A

agonist at GABA-B

monotherapy for spasticity 2/2 CNS disease

could also use Tizanidine (a2 agonist)

36
Q

essential tremor

A

most common movement disorder

slow, progressive, symmetric postural/kinetic tremor in UE

AD inheritance

tx propanolol