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21hydroxylasedeficiency diagnosis endocrinology genetics hyperammonemia pediatrics
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
major sources of ammonia ... production of ammonia ... Reye syndrome (Peds ... #Pathophysiology ... Hyperammonemia #Differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds
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