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diagnosis pediatrics peds iem inbornerrors metabolism neonatology nicu 21hydroxylasedeficiency 21ohd allergy antiarrhythmics cardiology classes differential endocrinology hypersensitivity laboratory metabolicemergency patterns
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... Peds #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Peds #Pediatrics #Table ... #NICU #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 ... maintains appropriate ion ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Hypersensitivity Types and Their Mechanisms Type I - lgE - Soluble antigen - Allergen-specific lgE antibodies bind
blood types or during ... Hypersensitivity #Types #Classification ... #Pathophysiology ... Diagnosis #Reactions #Table
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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