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21hydroxylasedeficiency algorithm diagnosis genetics pathophysiology peds shortstature
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD ... #peds #pediatrics
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis ... Hypothyroidism • Congenital ... #ShortStature #Differential ... Diagnosis #Algorithm #endocrinology ... #causes #pediatrics
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