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endocrinology pediatrics 21hydroxylasedeficiency 21ohd adrenal antiarrhythmics cah classification congenitaladrenalhyperplasia diagnosis genetics pharmacology phases treatment
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... #treatment #Peds ... Endocrinology #Adrenal #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 ... • 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 ... inotropy) ACCP Cardiology ... Classification #Classes ... #pathophysiology ... #phases #cardiology
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