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diagnosis differential 21hydroxylasedeficiency genetics hypertension indications pathophysiology pediatrics peds secondary thyroid workup
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 ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD
Hyperthyroidism Overview Clinical Manifestation of Hyperthyroidism: • Fatigue • Weight loss • Heat intolerance • Depression, nervousness
Hyperthyroidism ... Overview Clinical ... #causes #diagnosis ... #differential #endocrinology ... #signs #symptoms
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
hypertension and signs ... 109 mm Hg) with clinical ... renal bruit or signs ... Vasculitis • Endocrinologic ... : Hypothyroidism
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