STEP 1 Flashcards
Abdominal pain, ascites, hepatomegaly
Budd-Chiari syndrome (posthepatic venous thrombosis)
Achilles tendon xanthoma
Familial hypercholesterolemia (low LDLr signaling)
Adrenal hemorrhage, hypotension, DIC
Waterhouse-Friderichesen syndrome (meningococcemia)
Anterior “drawer” sign
Anterior cruciate ligament injury
Arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints
Marfan syndrom (fibrillin defect)
Athlete with polycythemia
Secondary to erythropoeitin injection
Back pain, night sweats, fever, weight loss
Pott disease (vertebral TB)
Bilateral hilar adenopathy, uveitis
Sarcoidosis (noncaseating granulomas)
Blue sclera
Osteogenesis imperfecta (type I collagen defect)
Bluish line on gingiva
Byron line (lead poisoning)
Bone pain, bone enlargement, arthritis
Paget disease of the bone (increased osteoblastic and osteoclastic activity)
Bounding pulses, diastolic heart murmur, head bobbing
Aortic regurgitation
Butterfly facial rash and Raynaud phenomenon in a young female
System lupus erythematosus
Cafe-au-lait spots, Lish nodules (Irish hamartoma)
Neurofibromatosis type 1 (+ pheochromocytoma, optic glioma
Café-Au-Lait spots, polyostotic fibrous displace, precocious puberty, multiple endocrine abnormalities
McCune-Albright syndrome (mosaic G protein signaling mutation
Calf pseudohypertrophy
Musclar dystrophy (most commonly Duchenne): X linked recessive deletion of dystrophin gene
Cherry red spots on macula
Tay-Sachs (ganglioside accumulation) or Niemann Pick (sphingomyelin accumulation), central retinal artery occlusion
Chest pain on exertion
Angina (stable: with moderate exertion; unstable: with minimal exertion)
Chest pain, pericardial effusion/friction rub, persistent fever following MI
Dressler syndrome (autoimmune mediated post MI fibrinous pericarditis, 1-12 weeks after acute episode)
Child uses arms to stand up from squat
Gowers sign (Duchenne muscular dystrophy
Child with fever later develops rash on face that spreads to body
Slapped cheeks - erythema infectiosum/fifth disease disease: parvovirus B19
Chorea, dementia, caudate degeneration
Huntington disease (aut. dominant CAG repeat expansion)
Chronic exercise intolerance with myalgia, fatigue, painful cramps, myoglobinuria
Macrocell disease (muscle glycogen phosphorylase deficiency)
Cold intolerance
hypothyroidism