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21hydroxylasedeficiency cushings diagnosis genetics hypercortisolism pathophysiology peds signs symptoms
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 ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD ... #peds #pediatrics
Cushing's Syndrome - Hypercortisolism - Diagnosis and Clinical Features 1) Skin • Thin, easily bruisable skin with
Cushing's Syndrome ... Diagnosis and Clinical ... is decreased), hypernatremia ... ↑ 24-hour urine ... signs #symptoms #endocrinology
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