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pediatrics 21hydroxylasedeficiency 21ohd dehydration endocrinology genetics management pathophysiology physicalexam sepsis stepwise
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Peds #Pediatrics
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
American College of Critical ... hemodynamic support in infants ... #Shock #Algorithm ... #CriticalCare # ... Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds
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