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21hydroxylasedeficiency 21ohd algorithm dehydration endocrinology genetics heartdisease infant management neonatal neonates pathophysiology physicalexam
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates Neonates with undiagnosed congenital
Algorithm for the Evaluation ... with nonspecific symptoms ... HeartDisease #Algorithm #Evaluation ... Neonates #Neonatal #Peds ... #Pediatrics #Cardiology
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
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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