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21hydroxylasedeficiency 21ohd criticalcare dehydration endocrinology genetics pathophysiology pediatric sepsis stepwise supraventricular svt tachycardia treatment
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Extremities #PhysicalExam ... #Signs #Symptoms ... #Shock #Infant ... #Dehydration #Peds ... #Pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... rate changes • Infants ... Signs of shock or ... #Algorithm #peds
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
Care Medicine algorithm ... hemodynamic support in infants ... #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
deficiencies present in infants ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
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