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peds diagnosis neonatal bhutani nomogram risk stratification thresholds neurotoxicity pathophysiology signssymptoms algorithm antenatal bilirubinemia complications counseling decisionaid diabetes diabetic differential
Approach to Neonatal Jaundice Causes of pathologic hyperbilirubinemia can be classified as due to (1) increased bilirubin
Approach to Neonatal ... Jaundice Causes ... of pathologic hyperbilirubinemia ... Diagnosis #Peds #Pediatrics ... #Neonatal #Jaundice
Threshold for Initiating Exchange Transfusion by Risk Stratum. Bhutani et al. Pediatrics. 1999. #Peds #Pediatrics #Diagnosis #Management
Pediatrics. 1999 ... #Peds #Pediatrics ... #Diagnosis #Management ... #Neonatal #Jaundice ... #Hyperbilirubinemia
Top tips for triaging and treating kids with Pitt Hopkins Syndrome #Diagnosis #Management #PatientInfo #Peds #Pediatrics #PittHopkins
with Pitt Hopkins Syndrome ... #Diagnosis #Management ... #PatientInfo #Peds ... #Pediatrics #PittHopkins ... #Syndrome #PTHS
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 ... #Hyperbilirubinemia
Risk Stratification for Developing Severe Hyperbilirubinemia. Bhutani et al. Pediatrics. 1999. In general, babies at low-risk and
Developing Severe Hyperbilirubinemia ... Pediatrics. 1999 ... #Peds #Pediatrics ... #Management #Neonatal ... #Jaundice #Hyperbilirubinemia
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... Poor suckling -> Neonatal ... #PraderWilli #Syndrome ... pathophysiology #peds #pediatrics
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
Diabetic #Mother #Pediatrics ... Pathophysiology #Maternal ... #Gestational #PatientInfo ... #Management #Obstetrics
Kleefstra Syndrome is a rare genetic disorder, caused by a EHMT-1 gene deletion or mutation. Most kids
Kleefstra Syndrome ... with Kleefstra Syndrome ... #Diagnosis #Management ... #PatientInfo #Peds ... #Pediatrics #Kleefstra
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