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peds 21ohd algorithm genetics management pathophysiology pediatric supraventricular svt tachycardia
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Monitors, Pads AP Stable ... Signs of shock or ... Algorithm #peds #Pediatric ... #treatment
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