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peds diagnosis cardiology iem inbornerrors management metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd algorithm anomaly differential ebstein encephalopathy endocrinology fallot hie
Hypoxic-ischemic encephalopathy (HIE) #HypoxicIschemic #encephalopathy #HIE #Neonatal #Peds #Pediatrics #Pathophysiology
encephalopathy #HIE #Neonatal ... #Peds #Pediatrics ... #Pathophysiology
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... of information: Pediatrics ... , UpToDate #Pediatrics ... MetabolicEmergency #Genetics ... #Pathophysiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Poor suckling -> Neonatal ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #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 #NICU #Genetics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... cardiology #peds #pediatrics
Ebstein Anomaly • Prevalence • Pathophysiology • Presentation • Physical Examination Findings • Initial Management •
Prevalence • Pathophysiology ... • Surgery in Neonates ... management #cardiology #pediatrics
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
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