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21hydroxylasedeficiency 21ohd genetics management pathophysiology pediatric supraventricular svt tachycardia
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... • Abrupt rate changes ... Signs of shock or ... #peds #Pediatric ... #treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Labia major & minor ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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