13 results
Causes of Respiratory Distress in the Newborn - Differential Diagnosis Algorithm
Premature Newborn
 - Normal CXR:
Distress in the Newborn ... Algorithm Premature Newborn ... Hemorrhage* • Hypoglycemia ... Tachypnea of the Newborn ... #Causes #Peds #Pediatrics
Infant of a Diabetic Mother - complications - pathophysiology learning schema
Information source: UpToDate

#Infant #Diabetic #Mother #Pediatrics
complications - pathophysiology ... Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds #Newborn
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm
Maternal Related:
 • Drugs (Ex. SSRI)
 •
Depressed / Lethargic Newborn ... Hypothermia • Hypoglycemia ... Depressed #Lethargic #Newborn ... #Causes #Peds #Pediatrics
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds #Newborn
Causes of Cyanosis in the Newborn - Differential Diagnosis Algorithm
Peripheral Only:
 • Poor Perfusion
 • Acrocyanosis
Hemoglobinopathy:
Cyanosis in the Newborn ... Total Anomalous Pulmonary ... #Cyanosis #Newborn ... #Causes #Peds #Pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Total Anomalous Pulmonary ... Classification • Pathophysiology ... Total #Anomalous #Pulmonary ... cardiology #peds #pediatrics
Truncus Arteriosus
 • Basic Information
 • Embryology
 • Associated anomalies
 • Pathophysiology/Presentation
 • Pre-operative management
 •
anomalies • Pathophysiology ... Cardiomegaly, increased pulmonary ... cardiology #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
sleep apnea, cor pulmonale ... 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
Hyperkalemia, Hypoglycemia ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Because they have decreased glycogen and fat stores, small for gestational age (SGA) babies are particularly
particularly prone to hypoglycemia ... #clinical #newborn ... #peds #pediatrics