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diagnosis 21hydroxylasedeficiency alte brue child childhood differential endocrinology event genetics immunization lifethreatening limping nwb pathway
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... , vomiting • Late ... #pathophysiology ... endocrinology #peds ... #pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Differential Diagnosis Algorithm ... Disturbances Neurologic ... #Causes #Peds # ... Pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
& seizures are late ... hemorrhagic rash; symptoms ... bacteremia are late ... #Immunization #peds ... #pediatrics #pathophysiology
THE LIMPING OR NON-WEIGHT BEARING CHILD PATHWAY RED FLAGS - In all cases there are specific markers which
FLAGS - In all cases ... splenomegaly, abnormal neurology ... #Limping #NWB #Algorithm ... Pathway #Child #Peds ... #Pediatrics #Diagnosis
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