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diagnosis pathophysiology 21hydroxylasedeficiency 21ohd antiarrhythmics cardiology causes differential dmd duchenne endocrinology features hyponatremia musculardystrophy pediatrics peds pharmacology phases signs
Classification, Differential Diagnosis, and Features of Hyponatremia According to Volume Status Hypervolemic hypernatremia - CHF
Classification, ... deficit - Salt-losing ... #Hyponatremia #Classification ... Differential #Diagnosis #Table ... #Causes
Duchenne Muscular Dystrophy (DMD) The term "Muscular dystrophy" refers to a group of inherited progressive muscle disorders.
Muscular Dystrophy is named ... defects in the gene coding ... brain. 1 in 3 cases ... Features #Signs #Genetics
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 ... pathophysiology #genetics
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Transient K+ efflux moving ... Vaughan Williams Classification ... : CLASS 1 - Sodium ... reduce speed of ion ... #Pharmacology #Classification
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