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diagnosis genetics brue cardiology iem inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd aortic aorticvalve bicuspid blue briefresolved causes congenital cyanotic
Congenital Heart Disorders - Classification and Differential Algorithm - Amy Chung, MD, MSc @AmyChung #Congenital #Heart #Disorders
and Differential ... Algorithm - ... #Differential # ... Algorithm #Diagnosis ... #Peds #Pediatrics
BRUE (Brief Resolved Unexplained Event) Algorithm ALTE (Apparent Life Threatening Event) is out, replaced with a new
ALTE (Apparent ... definition and classification ... Diagnosis #Management #Peds ... #Pedatrics #BRUE ... #ALTE
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... #Diagnosis #Algorithm ... #Differential # ... Neonatology #Peds ... #Pediatrics #Table
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... • Classifications ... Epidemiology • Clinical ... AorticValve #cardiology #peds ... #pediatrics
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Threatening Event (ALTE ... ) - Differential ... Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
workup 1) Clinical ... - 25% genetic component ... MNCD #Dementia #Differential ... #Subtypes #Classification ... Workup #Diagnosis #Geriatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... , elevation of ALT ... purposes of this algorithm ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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