infertility pediatrics diagnosis clinical neurology algorithm dystrophy alte sign 21ohd - GrepMed

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2 results

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 ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics

Evaluation of suspected incomplete Kawasaki Disease

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

if they have no clinical ... , elevation of ALT ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki

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