Pediatric Vital Signs causes clinical peds algorithm management infant stepbystep disease 21ohd

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics

Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7

Infants ≤6 months ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki ... #Algorithm

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