Rapid Review - Set 04 - Sheet1 Flashcards
Polyuria, renal tubular acidosis type II, growth failure, electrolyte imbalances, hypophosphatemic rickets
Fanconi’s syndrome (proximal tubular reabsorption defect)
Positive anterior “drawer sign”
ACL injury
Pruritic, purple, polygonal planar papules and plaques (6 Ps)
Lichen planus
Ptosis, miosis, anhidrosis
Horner’s Syndrome (sympathetic chain lesion)
Pupil accomodates but doesn’t react
Argyll Robertson pupil (neurosyphilis)
Rapidly progressive leg weakness that ascends following GI/upper respiratory infection
Guillan-Barre syndrome (acute autoimmune inflammatory demyelinating polyneuropathy)
Rash on palms and soles
Coxsackie A, Secondary Syphilis, Rocky Mountain Spotted Fever
Recurrent colds, unusual eczema, high serum IgE
Hyper IgE Syndrome (Job’s Syndrome: Neutrophil Chemotaxis Abnormality)
Red currant jelly sputum in alcoholic or diabetic patients
Klebsiella pneumonia
Red currant jelly stools
Adults: acute mesenteric ischemia; Children: Intussusception
Red, itchy, swollen rash of nipple/areola
Paget’s Disease of the breast (represents underlying neoplasm)
Red urine in the morning, fragile RBCs
Paroxysmal nocturnal hemoglobinuria
Renal cell carcinoma (bilateral), hemangioblastomas, angiomatosis, pheochromocytoma
von-Hippel-Lindau disease (dominant tumor suppressor gene mutation)
Resting tremor, rigidity, akinesia, postural instability
Parkinson’s disease (Nigrostriatal DA depletion)
Retinal hemorrhages with pale centers
Roth’s spots (bacterial endocarditis)
Severe jaundice in neonate
Crigler-Najjar syndrome (congenital unconjugated hyperbilirubinemia)
Severe RLQ pain with palpation of LLQ
Rovsing’s sign (acute appendicitis)
Severe RLQ with rebound tenderness
McBurney’s Sign (appendicitis)
Short stature, increased incidence of tumors/leukemia, aplastic anemia
Fanconi’s Anemia (genetic loss of DNA crosslink repair; often progresses to AML)
Single palmar crease
Simian crease (Down syndrome)
Situs inversus, chronic sinusitis, bronchiecstasis, infertility (immobile sperm)
Kartagener’s syndrome (dynein arm defect affecting cilia)
Skin hyperpigmentation, hypotension, fatigue
Addison’s disease (Primary adrenocortical insufficiency causes increased ACTH and increased alpha-Melanocyte Stimulating Hormone production)
Slow, progressive, muscle weakness in boys
Becker’s muscular dystrophy (X-linked missense mutation in dystrophin; less severe than Duchenne’s)
Small, irregular red spots on buccal/lingual mucosa with blue-white centers
Koplik spots (measles; rubeola virus)