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21hydroxylasedeficiency clinical cullen cullensign em emergencymedicine fm genetics icu pancreatitis pediatrics peds peritonitis surgery
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
Bruising in the skin ... Pathophysiology: ... onset of other symptoms ... cullen #clinical #image ... #peritonitis #IM
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