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21hydroxylasedeficiency button diagnosis endocrinology genetics ingestion pathophysiology peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics
Pediatric Button Battery Ingestion Most serious BB ingestions are not witnessed. Therefore, have a low threshold for
Pediatric Button ... Battery Ingestion ... children with symptoms ... #Ingestion #toxicology ... #diagnosis #management
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