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21hydroxylasedeficiency cardiology cardiomyopathy cullen cullensign em emergencymedicine endocrinology fm genetics icu im image management pancreatitis pathophysiology pediatrics peripartum 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 ... enzyme 21-OHase causes ... deficiencies present in infants ... , vomiting • Late ... endocrinology #peds
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
conditions that cause ... necrosis, ectopic pregnancy ... , or other causes ... requiring urgent medical ... It's typically a late
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Differential Diagnosis ... Period • Breast-feeding ... deteriorating on medical ... teratogenic GDMT meds
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