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pediatrics 21hydroxylasedeficiency 21ohd brue clinical cullen cullensign diagnosis differential emergencymedicine endocrinology fm genetics icu im image lifethreatening pancreatitis peritonitis surgery
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Life Threatening Event ... (ALTE) - Differential ... Diagnosis Algorithm ... #Causes #Peds #
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
conditions that cause ... Pathophysiology: ... pregnancy, or other causes ... In summary, Cullen's ... #cullensign #em
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