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pathophysiology signs 21hydroxylasedeficiency algorithm disease endocrinology genetics hepatology incomplete kawasaki liverfailure otitismedia physicalexam
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Findings Autosomal ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... in Children #Cirrhosis ... #LiverFailure #Signs ... #Findings #Diagnosis ... #Peds #Pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... Findings (in Children ... pathophysiology #diagnosis ... #symptoms #signs ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... Check for classic findings ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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