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pathophysiology signs 21hydroxylasedeficiency 21ohd diagnosis disease endocrinology features kawasaki otitismedia praderwilli syndrome timeline
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Syndrome Signs/Symptoms ... PraderWilli #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... Respiratory Tract Infection ... pathophysiology #diagnosis #symptoms ... #signs #peds #pediatrics
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
- Timeline of Clinical ... - Conjunctival infection ... Features #Signs #Symptoms ... #Peds #Pediatrics
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