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21hydroxylasedeficiency cardiology cardiomyopathy diagnosis differential genetics pediatrics peds restrictive
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 ... urine output • Hirsutism ... #pathophysiology ... #genetics #endocrinology
Restrictive Cardiomyopathy - Diagnosis and Causes Clinical: Dyspnea, Exercise Intolerance, ↑ "Right Sided-Symptoms" (ascites, hepatomegaly, ↑↑peripheral edema) Physical
Diagnosis and Causes ... ↑ "Right Sided-Symptoms ... Hyper-eosinophilc Syndrome ... Non-lnfiltrative: Idiopathic, Diabetic ... #algorithm
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