12 results
Threshold for Initiating Exchange Transfusion by Risk Stratum. Bhutani et al. Pediatrics. 1999.

#Peds #Pediatrics #Diagnosis #Management
Threshold for Initiating ... Pediatrics. 1999 ... #Peds #Pediatrics ... #Diagnosis #Management ... #Neonatal #Jaundice
Signs and Symptoms of Respiratory Distress Through the Years. 

#signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #differential #neonatal ... #pediatrics #adult ... #peds #pulmonary ... respiratory #distress #causes
Indications for Transfusion of Platelets in Neonates

#Management #Peds #Pediatrics #Platelets #Transfusion #Plateletpheresis #Thresholds #NonBleeding #Surgery
of Platelets in Neonates ... #Management # ... Peds #Pediatrics ... Plateletpheresis #Thresholds
Assess risk for developing subsequent neurotoxicity.

This will tell you: a) phototherapy or b) exchange transfusion

#Peds #Pediatrics
transfusion #Peds ... #Pediatrics #Diagnosis ... #Management #Neonatal ... Neurotoxicity #Thresholds
Ebstein Anomaly
 • Prevalence
 • Pathophysiology
 • Presentation
 • Physical Examination Findings
 • Initial Management
 •
Prevalence • Pathophysiology ... Findings • Initial Management ... • Surgery in Neonates ... #cardiology #pediatrics ... #peds
Risk Stratification for Developing Severe Hyperbilirubinemia. Bhutani et al. Pediatrics. 1999.

In general, babies at low-risk and
Pediatrics. 1999 ... #Peds #Pediatrics ... #Management #Neonatal ... Nomogram #RiskZones #Thresholds
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... Pre-Operative Management ... #cardiology #peds ... #pediatrics #summary
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Poor suckling -> Neonatal ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... While the pathophysiology ... #PhysicalExam #Pediatrics ... #Peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics