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childhood diagnosis disease genetics incomplete kawasaki praderwilli syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Incr Skeletal fractures ... • Short stature ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
Childhood Immunization ... Tetanus Toxin -> Spores ... lymph -> Koplik's spots ... #peds #pediatrics ... #pathophysiology
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
old on day ≥7 of fever ... effusion, or z scores ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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