8 results
Infant of a Diabetic Mother - complications - pathophysiology learning schema
Information source: UpToDate

#Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... complications - pathophysiology ... : UpToDate #Infant ... #Pediatrics #Neonatology ... Complications #Peds
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes ... algorithm #Infant ... #Pediatrics #Neonatology ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
This is part of acrocyanosis ... The skin in this infant ... #clinical #photo ... #peds #pediatrics ... perioral #cyanosis #acrocyanosis
Acrocyanosis- As this infant is transitioning, the blue color on the feet is starting to resolve
Acrocyanosis- As ... this infant is ... #clinical #photo ... #peds #pediatrics ... #newborn #acrocyanosis
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... diagnosis #management #cardiology ... #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... Obesity -> Type 2 diabetes ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
...this infant is large for gestational age (LGA) with a birth weight of about 9 1/2
...this infant is ... of diabetic mothers ... though mild in this photo ... newborn #LGA #large #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 ... endocrinology #peds ... #pediatrics