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21hydroxylasedeficiency antiarrhythmics cardiology classes endocrinology genetics pediatrics peds 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 ... maintains appropriate ion ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Transient K+ efflux moving ... Vaughan Williams Classification ... reduce speed of ion ... #Pharmacology #Classification ... #Classes #pathophysiology
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