First Aid Rapid Review Flashcards
(478 cards)
Abdominal pain, ascites, hepatomegaly
Budd-Chiari syndrome (posthepatic venous thrombosis)
Achilles tendon xantoma
Familial Hypercholesterolemia (reduced LDL receptor signalling)
Adrenal hemorrhage, hypotension, DIC
Waterhouse-Friderichsen syndrom (meningococcemia)
Arachnodactyly, lens dislocation, aortic dissection, hyperflexible joints
Marfan’s syndrome (fibrillin defect)
Athlete w/ polycythemia
secondary to erythropoeitein injection
back pain, fever, night sweats, weight loss
Pott’s Disease (vertebral TB)
Bilateral hilar adenopathy, uveitis
sarcoidosis (noncaseating granulomas)
blue sclera
osteogenesis imperfecta (type 1 collagen defect)
bluish line on gingiva
Burton’s lines (lead poisoning)
bone pain, bone enlargement, arthritis
Paget’s disease of bone (increased osteoblastic and osteoclastic activity)
Bounding pulses, diastolic heart murmur, head bobbing
Aortic regurgitation
Butterfly facial rash and Raynaud’s phenomenon in a young female
SLE
Cafe au lait spots, Lisch nodules (iris hamartoma)
NF type 1 (+pheochromocytoma, optic gliomas)
Cafe au lait spots, polyostotic fibrous dysplasia, precocious puberty, multiple endocrine abnormailities
McCune-Albright syndrome (Mosaic G-protein signalling mutation)
Calf psuedohypertrophy
muscular dystrophy (most commonly Duchenne’s): X-linked recessive deletion of dystrophin gene
Cherry-red spot on macula
Tay-Sachs (ganglioside accumulation) or Neimann-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’s syndrome (autoimmune-mediated post-MI fibrinous pericarditis, 1-12 weeks after acute episode)
Child uses arms to stand up from squat
Gower’s sign (Duchenne muscular dystrophy)
Child with fever later develops red rash on face that spreads to the body
Slapped Cheeks (erythemea infectiosum/fifth disease: parvovirus B19)
Chorea, dementia, caudate degeneration
Huntington’s Disease (autosomal-dominant CAG repeat expansion)
chronic exercise intolerance with myalgia, fatigue, painful cramps, myoglobinuria
McArdle’s disease (muscle glycogen phosphorylase deficiency)
Cold intolerance
hypothyroidism
conjugate lateral gaze palsy, horizontal diplopia
internuclear ophthalmoplegia (damage to MLF; bilateral [multiple sclerosis], unilateral [stroke])