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21hydroxylasedeficiency causes differential genetics hypercortisolism hypertension indications pediatrics peds secondary symptoms syndrome workup
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Cushing's Syndrome - Hypercortisolism - Diagnosis and Clinical Features 1) Skin • Thin, easily bruisable skin with
Hypercortisolism - Diagnosis ... Cataracts Labs: Hypokalemia ... the abdomen for adrenal ... #signs #symptoms ... #endocrinology
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
and Differential Diagnosis ... hypertension and signs ... bruit or signs ... Vasculitis • Endocrinologic ... Hypercalcemia, Cushing's
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