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21hydroxylasedeficiency 21ohd antiarrhythmics classes endocrinology genetics pediatrics pharmacology phases
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 ... • Early: decr feeding ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Transient K+ efflux moving ... Vaughan Williams Classification ... inotropy) ACCP Cardiology ... #Classes #pathophysiology ... #phases #cardiology
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