11 results
diagnosis hyperbilirubinemia management bhutani neonatal nomogram risk stratification iem inbornerrors metabolism neonatology neurotoxicity nicu table 21hydroxylasedeficiency 21ohd algorithm cardiology childhood
Threshold for Initiating Exchange Transfusion by Risk Stratum. Bhutani et al. Pediatrics. 1999. #Peds #Pediatrics #Diagnosis #Management
Threshold for Initiating ... Pediatrics. 1999 ... #Peds #Pediatrics ... Management #Neonatal #Jaundice ... Neurotoxicity #Thresholds
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Neonatology #Peds ... #Pediatrics #Table
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 ... #NICU #Genetics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... management #cardiology #peds ... #pediatrics #treatment
Inherited forms of Hyperbilirubinemia Major pathways involved in bilirubin production, conjugation, and excretion. Notes: Both the UB
Decreased MRP2 - Conjugated ... Decreased OATP1B - Conjugated ... Hyperbilirubinemia #pathophysiology ... congenital #hepatology #pediatrics ... #peds
Assess risk for developing subsequent neurotoxicity. This will tell you: a) phototherapy or b) exchange transfusion #Peds #Pediatrics
transfusion #Peds ... #Pediatrics #Diagnosis ... Management #Neonatal #Jaundice ... Neurotoxicity #Thresholds
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Risk Stratification for Developing Severe Hyperbilirubinemia. Bhutani et al. Pediatrics. 1999. In general, babies at low-risk and
Pediatrics. 1999 ... #Peds #Pediatrics ... Management #Neonatal #Jaundice ... Nomogram #RiskZones #Thresholds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
anorexia, nausea, jaundice ... #Immunization #peds ... #pediatrics #pathophysiology
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