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21hydroxylasedeficiency 21ohd cardiology criticalcare endocrinology evaluation genetics heartdisease neonatal neonates pathophysiology pediatric sepsis stepwise supraventricular svt tachycardia treatment
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates Neonates with undiagnosed congenital
Algorithm for the ... Evaluation and Management ... with nonspecific symptoms ... Neonates #Neonatal #Peds ... #Pediatrics #Cardiology
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... Signs of shock or ... #Algorithm #peds ... #Pediatric #treatment
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
Care Medicine algorithm ... 70% (* except congenital ... #Shock #Algorithm ... #CriticalCare #Peds ... #Pediatrics #Sepsis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
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