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21ohd cullen cullensign emergencymedicine endocrinology fm genetics icu im image pancreatitis pediatrics peritonitis surgery
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 ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... endocrinology #peds
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
Pathophysiology: ... Clinical Significance ... a significant clinical ... #cullensign #em ... peritonitis #IM #FM #ICU
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