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21hydroxylasedeficiency clinical cullen cullensign emergencymedicine fm icu image pediatrics peds peritonitis surgery
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
Pathophysiology: ... It's typically a late ... #cullensign #em ... #pancreatitis #cullen ... #peritonitis #IM
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