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diagnosis management neonatology nicu febrile fever lp risk stepbystep stratification diabetes diabetic gestational idm iem inbornerrors maternal metabolism mother newborn
Validation of the Step-By-Step Approach to Febrile Infants #Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
Diagnosis #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep ... #Algorithm #LP ... #Antibiotics #Risk
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... Mother - complications ... - pathophysiology ... Diabetic #Mother #Pediatrics ... #Peds #Newborn
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... #Mother #Pediatrics ... #Maternal #Complications ... #Peds #Newborn
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... #Neonatology #Peds
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
The Febrile Infant Step-by-Step Algorithm This is an algorithm developed by European emergency physicians to identify low-risk
The Febrile Infant ... puncture nor empiric antibiotic ... EBM #Management #Pediatrics ... #Peds #Febrile ... #Antibiotics #Risk
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... Diagnosis #Management #Pediatrics ... #Peds #Febrile ... #Algorithm #LP ... #Antibiotics #Risk
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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