Iron table classification dosing algorithm pacemaker coding classes pathophysiology genetics

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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 ... #genetics #endocrinology

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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