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21hydroxylasedeficiency cardiology cardiomyopathy diagnosis endocrinology management pathophysiology pediatrics peripartum treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Hypoglycemia • Early ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics ... endocrinology #peds
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Genetic predisposition ... estrogen products early ... postpartum • Consider early ... teratogenic GDMT meds
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