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pediatrics 21hydroxylasedeficiency 21ohd antiarrhythmics cardiology causes clinical cullen cullensign diagnosis differential em emergencymedicine endocrinology event fm genetics icu im image
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Threatening Event (ALTE ... Differential Diagnosis Algorithm ... #BRUE #Differential ... #Diagnosis #Algorithm ... #Causes #Peds #
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Antiarrhythmics Pharmacology Summary ... Transient K+ efflux moving ... Phase 4 - True Resting ... Vaughan Williams Classification ... #Classes #pathophysiology
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
characterized by a blue ... Pathophysiology: ... pregnancy, or other causes ... It's typically a late ... In summary, Cullen's
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