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diagnosis 21hydroxylasedeficiency 21ohd causes genetics hypertension indications management nephrology peds secondary syndrome workup
Gitelman Syndrome Overview What? • Inherited (AR) hypokalemic salt-losing tubulopathies affecting the thiazide-sensitive sodium chloride cotransporter • Gitelman's syndrome
tubule (DCT) Clinical ... Family history of hypokalemia ... • Unexplained hypokalemia ... pressure Labs: • Hypokalemia ... #Hypokalemia
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... wasting crisis & hyperkalemia ... Complications: • Hyperkalemia ... #genetics #endocrinology ... #peds #pediatrics
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
disorders including hypokalemia ... 109 mm Hg) with clinical ... Vasculitis • Endocrinologic ... Hyperthyroidism, Hypercalcemia ... Neurologic disorders
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