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USMLE Step 1 Rapid Review Questions and Answers 100% Pass

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USMLE Step 1 Rapid Review Questions and Answers 100% Pass abdominal pain, ascites, hepatomegaly - Budd-Chiari syndrome Familial hypercholesterolemia - achilles tendon xanthoma adrenal hemorrhage, hypotension, DIC - Waterhouse-Friderichsen syndrome biochemistry of Marfan's syndrome - fibrillin defect posthepatic venous thrombosis - Budd-Chiari syndrome Familial hypercholesterolemia biochemistry - decrease in LDL receptor signaling Waterhouse-Friderichsen syndrome cause - meningococcemia arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints - Marfan's syndrome Athlete with polycythemia - EPO injection Pott's disease - vertebral TB 2100% Pass Guarantee Emilly Charlotte, All Rights Reserved © 2025 Pott's disease clinical presentation - back pain, fever, night sweats, weight loss Sarcoidosis main histological presentation - noncaseating granuloma bilateral hilar adenopathy + uveitis - sarcoidosis Osteogenesis imperfecta - type I collagen defect Blue sclera indicate what? - osteogenesis imperfecta Burton's line indicates what? - lead poisoning Burton's line - bluish line on gingiva Paget's disease of the bone biochemistry - increase in osteoblastic and osteoclastic activity bone pain, bone enlargement, arthritis - Paget's disease of the bone bounding pulses, diastolic heart murmur, head bobbing - aortic regurgitation butterfly facial rash, Raynaud's phenomenon in a young female - SLE Neurofibromatosis type I associated with what malignancies - pheochromocytoma, optic gliomas cafe-au-lait spots and Lisch nodules - Neurofibromatosis type I Lisch nodules - iris hemartoma 3100% Pass Guarantee Emilly Charlotte, All Rights Reserved © 2025 McCune-Albright syndrome biochemistry - mosaic continuous activation of stimulatory G protein cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine abnormalities - McCune-Albright syndrome Duchenne's muscular dystrophy - X-linked recessive deletion of dystrophin gene Calf pseduohypertrophy - Duchenne's muscular dystrophy clinical sign of Tay-Sach's, Niemann-Pick, or central retinal artery occlusion - Cherry-red spot on macula ganglioside accumulation - Tay-Sach's sphingomyelin accumulation - Niemann-Pick diseas

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Subido en
1 de marzo de 2025
Número de páginas
61
Escrito en
2024/2025
Tipo
Examen
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USMLE Step 1 Rapid Review
Questions and Answers 100% Pass


abdominal pain, ascites, hepatomegaly - ✔✔Budd-Chiari syndrome


Familial hypercholesterolemia - ✔✔achilles tendon xanthoma


adrenal hemorrhage, hypotension, DIC - ✔✔Waterhouse-Friderichsen syndrome


biochemistry of Marfan's syndrome - ✔✔fibrillin defect


posthepatic venous thrombosis - ✔✔Budd-Chiari syndrome


Familial hypercholesterolemia biochemistry - ✔✔decrease in LDL receptor signaling


Waterhouse-Friderichsen syndrome cause - ✔✔meningococcemia


arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints - ✔✔Marfan's

syndrome


Athlete with polycythemia - ✔✔EPO injection


Pott's disease - ✔✔vertebral TB




100% Pass Guarantee Emilly Charlotte, All Rights Reserved © 2025 1

,Pott's disease clinical presentation - ✔✔back pain, fever, night sweats, weight loss


Sarcoidosis main histological presentation - ✔✔noncaseating granuloma


bilateral hilar adenopathy + uveitis - ✔✔sarcoidosis


Osteogenesis imperfecta - ✔✔type I collagen defect


Blue sclera indicate what? - ✔✔osteogenesis imperfecta


Burton's line indicates what? - ✔✔lead poisoning


Burton's line - ✔✔bluish line on gingiva


Paget's disease of the bone biochemistry - ✔✔increase in osteoblastic and osteoclastic

activity


bone pain, bone enlargement, arthritis - ✔✔Paget's disease of the bone


bounding pulses, diastolic heart murmur, head bobbing - ✔✔aortic regurgitation


butterfly facial rash, Raynaud's phenomenon in a young female - ✔✔SLE


Neurofibromatosis type I associated with what malignancies - ✔✔pheochromocytoma,

optic gliomas


cafe-au-lait spots and Lisch nodules - ✔✔Neurofibromatosis type I


Lisch nodules - ✔✔iris hemartoma




100% Pass Guarantee Emilly Charlotte, All Rights Reserved © 2025 2

,McCune-Albright syndrome biochemistry - ✔✔mosaic continuous activation of

stimulatory G protein


cafe-au-lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine

abnormalities - ✔✔McCune-Albright syndrome


Duchenne's muscular dystrophy - ✔✔X-linked recessive deletion of dystrophin gene


Calf pseduohypertrophy - ✔✔Duchenne's muscular dystrophy


clinical sign of Tay-Sach's, Niemann-Pick, or central retinal artery occlusion -

✔✔Cherry-red spot on macula


ganglioside accumulation - ✔✔Tay-Sach's


sphingomyelin accumulation - ✔✔Niemann-Pick disease


Stable angina - ✔✔with moderate exercise


Unstable angina - ✔✔with minimal exertion


Angina - ✔✔chest pain on exertion


autoimmune-mediated post-MI fibrinous pericarditis 1-12 weeks after acute episode -

✔✔Dressler syndrome


Chest pain, pericardial effusion, friction rub, persistent fever following MI 1-12 weeks

after - ✔✔Dressler's syndrome




100% Pass Guarantee Emilly Charlotte, All Rights Reserved © 2025 3

, Gowers' sign associated with what disease? - ✔✔Duchenne muscular dystrophy


Gower's sign definition - ✔✔child uses arms to stand up from squat


"Slapped cheeks" - ✔✔erythema infectiosum/fifth disease


Erythema infectiosum/fifth disease - ✔✔parvovirus B19


child with fever later develops red rash on face that spreads to body - ✔✔erythema

infectiosum/fifth disease


autosomal-dominant CAG repeat expansion - ✔✔Huntington's disease


chorea, dementia, caudate degeneration - ✔✔Huntington's disease


muscle glycogen phosphorylase deficiency - ✔✔McArdle's syndrome


chronic exercise intolerance with myalgia, fatigue, painful cramps, myoglobinuria -

✔✔McArdle's disease


Cold intolerance may suggest what diagnosis? - ✔✔hypothyroidism


Lesion that causes internuclear ophthalmoplegia - ✔✔damage to MLF


Bilateral internuclear opthalmoplegia associated with what condition? - ✔✔multiple

sclerosis


cause of Unilateral internuclear opthalmoplegia - ✔✔stroke




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