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21hydroxylasedeficiency diagnosis differential genetics pathophysiology peds shortstature
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... • IGF-I Deficiency ... Panhypopituitarism Treatment ... #endocrinology ... #causes #pediatrics
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