UWORLD random 3/17 Flashcards
DM I sx
polyuria
polydipsia
polyphagia
fatigue
weight loss
delirium tx
haloperidol
lesions that cause ONLY inguinal LAD
medial LE
lesions that cause BOTH popliteal and inguinal LAD
lateral LE
Western Blot
protein
Southern Blot
DNA
Northern Blot
mRNA
Southwestern Blot
DNA-bound protein
CML genes
BCR-ABL fusion gene
t(9;22)
metabolism of v long fatty acid chains/branch chain at odd-numbered fatty acids
peroxisomes
Zellweger syndrome
peroxisomal disease
unable to form myelin in CNS
hypotonia, seizures, hepatomegaly, mental retardation, early death
refsum disease
peroxisomal disease
defect in a-oxidation
neuro disturbances from phytanic acid accumulation
tx = avoid chlorophyll
glossopharyngeal nerve
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
glossopharyngeal nerve lesions
loss of gag reflex
loss of sensation in upper pharynx, posterior tongue, tonsils, middle ear cavity
loss of taste in posterior 1/3 tongue
when b-hcg is detectable in serum
6-8 days after fertilization
implantation 6 days after fertilization, syncytiotrophoblast starts secreting b-HCG
when b-hcg is detectable in urine
14 days
RA pressure
<5
RV pressure
25/5
Pulm artery pressure
25/10
LA pressure
<12
capillary wedge
LV pressure
130/10
Aorta pressure
130/90
PE acid/base disturbance
hypoxemia
respiratory alkalosis
live attenuated oral poliovirus vaccine Sabin vs inactivated Salk
secretory IgA in intestinal lumen
ischemia on CT
hypodense
poorly delineated from surrounding tissue
post-ischemic brain injury timeline
48 h = red neurons
3-5 days = neutrophils
followed by monocytes
2 wks = cystic space replaces necrosis
gliosis (astrocytes form glial scar)
lipids in microglia
phagocytosis of disintegrated neurons, myelin, necrotic debris
myelin breakdown products
acute intermittent porphyria
AD
porphobilinogen deaminase deficiency (PBG –> HMB)
AIP sx
mostly asx
acute attcks = abdominal pain, vomiting, peripheral neuropathy, neuropsycho sx, reddish-brown urine
AIP tx
IV glucose or heme preps
downregulate ALA synthase activity (reduce toxic intermediate metabolites of heme synthesis)
avoid CYP450 inducers
normal CD4+ lymphocyte count
> 500
polymyositis sx
symmetrical prox muscle weakness
increased difficulty climbing stairs, getting up from chair, carrying heavy objects
polymyositis pathology
+ muscle enzymes (CK, aldolase)
autoantibodies (ANA, anti-Jo-1)
MHC 1 antigens on sarcolemma with CD8+ cytotoxic T-cells, myocytes
polymyositis biopsy
inflammation
necrosis
regeneration of muscle fibers
(patchy necrosis)
Baclofen
agonist at GABA-B
monotherapy for spasticity 2/2 CNS disease
could also use Tizanidine (a2 agonist)
essential tremor
most common movement disorder
slow, progressive, symmetric postural/kinetic tremor in UE
AD inheritance
tx propanolol