USMLE Step 1 Rapid Review
abdominal pain, ascites, hepatomegaly ------- ✔ CORRECT ANSWER ✓✓Budd-Chiari syndrome
Familial hypercholesterolemia ------- ✔ CORRECT ANSWER ✓✓achilles tendon xanthoma
adrenal hemorrhage, hypotension, DIC ------- ✔ CORRECT ANSWER ✓✓Waterhouse-
Friderichsen syndrome
biochemistry of Marfan's syndrome ------- ✔ CORRECT ANSWER ✓✓fibrillin defect
posthepatic venous thrombosis ------- ✔ CORRECT ANSWER ✓✓Budd-Chiari syndrome
Familial hypercholesterolemia biochemistry ------- ✔ CORRECT ANSWER ✓✓decrease in LDL
receptor signaling
Waterhouse-Friderichsen syndrome cause ------- ✔ CORRECT ANSWER ✓✓meningococcemia
arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints ------- ✔ CORRECT
ANSWER ✓✓Marfan's syndrome
Athlete with polycythemia ------- ✔ CORRECT ANSWER ✓✓EPO injection
Pott's disease ------- ✔ CORRECT ANSWER ✓✓vertebral TB
, Pott's disease clinical presentation ------- ✔ CORRECT ANSWER ✓✓back pain, fever, night
sweats, weight loss
Sarcoidosis main histological presentation ------- ✔ CORRECT ANSWER ✓✓noncaseating
granuloma
bilateral hilar adenopathy + uveitis ------- ✔ CORRECT ANSWER ✓✓sarcoidosis
Osteogenesis imperfecta ------- ✔ CORRECT ANSWER ✓✓type I collagen defect
Blue sclera indicate what? ------- ✔ CORRECT ANSWER ✓✓osteogenesis imperfecta
Burton's line indicates what? ------- ✔ CORRECT ANSWER ✓✓lead poisoning
Burton's line ------- ✔ CORRECT ANSWER ✓✓bluish line on gingiva
Paget's disease of the bone biochemistry ------- ✔ CORRECT ANSWER ✓✓increase in
osteoblastic and osteoclastic activity
bone pain, bone enlargement, arthritis ------- ✔ CORRECT ANSWER ✓✓Paget's disease of the
bone
bounding pulses, diastolic heart murmur, head bobbing ------- ✔ CORRECT ANSWER ✓✓aortic
regurgitation
butterfly facial rash, Raynaud's phenomenon in a young female ------- ✔ CORRECT ANSWER
✓✓SLE
,Neurofibromatosis type I associated with what malignancies ------- ✔ CORRECT ANSWER
✓✓pheochromocytoma, optic gliomas
cafe-au-lait spots and Lisch nodules ------- ✔ CORRECT ANSWER ✓✓Neurofibromatosis type I
Lisch nodules ------- ✔ CORRECT ANSWER ✓✓iris hemartoma
McCune-Albright syndrome biochemistry ------- ✔ CORRECT ANSWER ✓✓mosaic continuous
activation of stimulatory G protein
cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine
abnormalities ------- ✔ CORRECT ANSWER ✓✓McCune-Albright syndrome
Duchenne's muscular dystrophy ------- ✔ CORRECT ANSWER ✓✓X-linked recessive deletion of
dystrophin gene
Calf pseduohypertrophy ------- ✔ CORRECT ANSWER ✓✓Duchenne's muscular dystrophy
clinical sign of Tay-Sach's, Niemann-Pick, or central retinal artery occlusion ------- ✔ CORRECT
ANSWER ✓✓Cherry-red spot on macula
ganglioside accumulation ------- ✔ CORRECT ANSWER ✓✓Tay-Sach's
sphingomyelin accumulation ------- ✔ CORRECT ANSWER ✓✓Niemann-Pick disease
Stable angina ------- ✔ CORRECT ANSWER ✓✓with moderate exercise
, Unstable angina ------- ✔ CORRECT ANSWER ✓✓with minimal exertion
Angina ------- ✔ CORRECT ANSWER ✓✓chest pain on exertion
autoimmune-mediated post-MI fibrinous pericarditis 1-12 weeks after acute episode ------- ✔
CORRECT ANSWER ✓✓Dressler syndrome
Chest pain, pericardial effusion, friction rub, persistent fever following MI 1-12 weeks after ------
- ✔ CORRECT ANSWER ✓✓Dressler's syndrome
Gowers' sign associated with what disease? ------- ✔ CORRECT ANSWER ✓✓Duchenne muscular
dystrophy
Gower's sign definition ------- ✔ CORRECT ANSWER ✓✓child uses arms to stand up from squat
"Slapped cheeks" ------- ✔ CORRECT ANSWER ✓✓erythema infectiosum/fifth disease
Erythema infectiosum/fifth disease ------- ✔ CORRECT ANSWER ✓✓parvovirus B19
child with fever later develops red rash on face that spreads to body ------- ✔ CORRECT ANSWER
✓✓erythema infectiosum/fifth disease
autosomal-dominant CAG repeat expansion ------- ✔ CORRECT ANSWER ✓✓Huntington's
disease
chorea, dementia, caudate degeneration ------- ✔ CORRECT ANSWER ✓✓Huntington's disease
abdominal pain, ascites, hepatomegaly ------- ✔ CORRECT ANSWER ✓✓Budd-Chiari syndrome
Familial hypercholesterolemia ------- ✔ CORRECT ANSWER ✓✓achilles tendon xanthoma
adrenal hemorrhage, hypotension, DIC ------- ✔ CORRECT ANSWER ✓✓Waterhouse-
Friderichsen syndrome
biochemistry of Marfan's syndrome ------- ✔ CORRECT ANSWER ✓✓fibrillin defect
posthepatic venous thrombosis ------- ✔ CORRECT ANSWER ✓✓Budd-Chiari syndrome
Familial hypercholesterolemia biochemistry ------- ✔ CORRECT ANSWER ✓✓decrease in LDL
receptor signaling
Waterhouse-Friderichsen syndrome cause ------- ✔ CORRECT ANSWER ✓✓meningococcemia
arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints ------- ✔ CORRECT
ANSWER ✓✓Marfan's syndrome
Athlete with polycythemia ------- ✔ CORRECT ANSWER ✓✓EPO injection
Pott's disease ------- ✔ CORRECT ANSWER ✓✓vertebral TB
, Pott's disease clinical presentation ------- ✔ CORRECT ANSWER ✓✓back pain, fever, night
sweats, weight loss
Sarcoidosis main histological presentation ------- ✔ CORRECT ANSWER ✓✓noncaseating
granuloma
bilateral hilar adenopathy + uveitis ------- ✔ CORRECT ANSWER ✓✓sarcoidosis
Osteogenesis imperfecta ------- ✔ CORRECT ANSWER ✓✓type I collagen defect
Blue sclera indicate what? ------- ✔ CORRECT ANSWER ✓✓osteogenesis imperfecta
Burton's line indicates what? ------- ✔ CORRECT ANSWER ✓✓lead poisoning
Burton's line ------- ✔ CORRECT ANSWER ✓✓bluish line on gingiva
Paget's disease of the bone biochemistry ------- ✔ CORRECT ANSWER ✓✓increase in
osteoblastic and osteoclastic activity
bone pain, bone enlargement, arthritis ------- ✔ CORRECT ANSWER ✓✓Paget's disease of the
bone
bounding pulses, diastolic heart murmur, head bobbing ------- ✔ CORRECT ANSWER ✓✓aortic
regurgitation
butterfly facial rash, Raynaud's phenomenon in a young female ------- ✔ CORRECT ANSWER
✓✓SLE
,Neurofibromatosis type I associated with what malignancies ------- ✔ CORRECT ANSWER
✓✓pheochromocytoma, optic gliomas
cafe-au-lait spots and Lisch nodules ------- ✔ CORRECT ANSWER ✓✓Neurofibromatosis type I
Lisch nodules ------- ✔ CORRECT ANSWER ✓✓iris hemartoma
McCune-Albright syndrome biochemistry ------- ✔ CORRECT ANSWER ✓✓mosaic continuous
activation of stimulatory G protein
cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine
abnormalities ------- ✔ CORRECT ANSWER ✓✓McCune-Albright syndrome
Duchenne's muscular dystrophy ------- ✔ CORRECT ANSWER ✓✓X-linked recessive deletion of
dystrophin gene
Calf pseduohypertrophy ------- ✔ CORRECT ANSWER ✓✓Duchenne's muscular dystrophy
clinical sign of Tay-Sach's, Niemann-Pick, or central retinal artery occlusion ------- ✔ CORRECT
ANSWER ✓✓Cherry-red spot on macula
ganglioside accumulation ------- ✔ CORRECT ANSWER ✓✓Tay-Sach's
sphingomyelin accumulation ------- ✔ CORRECT ANSWER ✓✓Niemann-Pick disease
Stable angina ------- ✔ CORRECT ANSWER ✓✓with moderate exercise
, Unstable angina ------- ✔ CORRECT ANSWER ✓✓with minimal exertion
Angina ------- ✔ CORRECT ANSWER ✓✓chest pain on exertion
autoimmune-mediated post-MI fibrinous pericarditis 1-12 weeks after acute episode ------- ✔
CORRECT ANSWER ✓✓Dressler syndrome
Chest pain, pericardial effusion, friction rub, persistent fever following MI 1-12 weeks after ------
- ✔ CORRECT ANSWER ✓✓Dressler's syndrome
Gowers' sign associated with what disease? ------- ✔ CORRECT ANSWER ✓✓Duchenne muscular
dystrophy
Gower's sign definition ------- ✔ CORRECT ANSWER ✓✓child uses arms to stand up from squat
"Slapped cheeks" ------- ✔ CORRECT ANSWER ✓✓erythema infectiosum/fifth disease
Erythema infectiosum/fifth disease ------- ✔ CORRECT ANSWER ✓✓parvovirus B19
child with fever later develops red rash on face that spreads to body ------- ✔ CORRECT ANSWER
✓✓erythema infectiosum/fifth disease
autosomal-dominant CAG repeat expansion ------- ✔ CORRECT ANSWER ✓✓Huntington's
disease
chorea, dementia, caudate degeneration ------- ✔ CORRECT ANSWER ✓✓Huntington's disease