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algorithm diagnosis 21hydroxylasedeficiency 21ohd cirrhosis congenital endocrinology genetics heartdisease hepatology incomplete kawasaki liverfailure 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 ... Congenital Heart Disease ... with nonspecific symptoms ... Neonates #Neonatal #Peds ... #Pediatrics #Cardiology
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
features of Liver Disease ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #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 Findings ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Evaluation of suspected ... Check for classic findings ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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