7 results
diagnosis differential pediatrics 21hydroxylasedeficiency 21ohd alte antiarrhythmics brue cardiology conjugated endocrinology epilepsy event genetics hyponatremia jaundice lifethreatening pharmacology phases seizures
Classification, Differential Diagnosis, and Features of Hyponatremia According to Volume Status Hypervolemic hypernatremia - CHF
Classification, ... deficit - Salt-losing ... #Hyponatremia #Classification ... Differential #Diagnosis #Table ... #Causes
Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... Differential Diagnosis Algorithm ... Spells: • Breath-holding ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Differential Diagnosis Algorithm ... Aspiration • Breath-holding ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Classification of Jaundice Unconjugated hyperbilirubinemia (predominantly indirect bilirubin) • Increased bilirubin production (eg, hemolytic anemias, hemolytic reactions,
mutation in genes coding ... cholestasis, and some cases ... Hepatocellular Dysfunction ... miscellaneous causes ... #differential #causes
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... Spells: • Breath-holding ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
channels open leading ... Transient K+ efflux moving ... Vaughan Williams Classification ... #Pharmacology #Classification ... #Classes #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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
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