Satellite skin ucsdh signs differential causes symptoms em pathophysiology 21ohd genetics icu image

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

enzyme 21-OHase causes ... Signs/Symptoms/Complications ... cold & mottled skin ... #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 ... #cullensign #em ... cullen #clinical #image

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