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diagnosis algorithm management evaluation fever iem inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd admission assessment cardiology compensated decompensated diagram differential
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Evaluation of Pediatric ... Diagnosis #Management #EM ... #Peds #Trauma # ... PECARN #Algorithm #Ddxof
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
Rapid Pediatric Assessment Diagram: * Assessment of Appearance - Tone: Moves spontaneously, resists examination -
Rapid Pediatric ... Cyanosis #Diagnosis #EM ... #Peds #Rapid #Assessment ... Decompensated #Shock #Ddxof
Pathophysiology Pediatric Fever #Pathophys #Peds #Fever #Ddxof
Pathophysiology ... Pediatric Fever ... #Pathophys #Peds ... #Fever #Ddxof
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Evaluation and Management of Pediatric Fever #Diagnosis #Management #EM #Peds #Fever #Workup #Evaluation #Discharge #Admission #Algorithm
Management of Pediatric ... Diagnosis #Management #EM ... #Peds #Fever #Workup ... Admission #Algorithm #Ddxof
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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