Pediatrics pathophysiology newborn syndrome symptoms peds congenital diagnosis complications genetics 21hydroxylasedeficiency nicu counseling

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4 results

gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn

Diabetic #Mother #Pediatrics ... Neonatology #IDM #NICU ... #OBGYN #Diagnosis ... #Pathophysiology ... #Peds #Newborn

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

#Infant #Diabetic #Mother #Pediatrics

- pathophysiology ... Diabetic #Mother #Pediatrics ... Neonatology #IDM #NICU ... #OBGYN #Diagnosis ... #Peds #Newborn

Prader-Willi Syndrome: Pathogenesis and clinical findings
• Maternal uniparental disomy: inheriting 2 copies of maternal chromosome

Prader-Willi Syndrome ... Signs/Symptoms ... /Complications: ... #genetics #pathophysiology ... #peds #pediatrics

21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

also known as "congenital ... Signs/Symptoms/Complications ... #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

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