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Updated: Jun 3, 2025

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Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
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Case report: Kabuki syndrome and persistent hypoglycemia in neonates
Osama Y Safdar1,2,3, Miral M Abddulghfar2,3, Renad N Saaty2,3
1Pediatric Nephrology Center of Excellence, King Abdluaziz University Hospital, Jeddah, Saudi Arabia.
Journal of Family Medicine and Primary Care
|January 10, 2025
Summary
Kabuki syndrome type 2, a rare genetic disorder, can cause severe neonatal hypoglycemia due to KDM6A gene mutations. Early diagnosis and treatment are crucial for preventing neurodevelopmental complications.
Area of Science:
- Genetics
- Pediatrics
- Endocrinology
Background:
- Kabuki syndrome (KS) is a rare congenital disorder with two types (KS1 and KS2), linked to KMT2D and KDM6A gene variants.
- KS presents with diverse abnormalities including developmental delay, distinctive facial features, and organ anomalies.
- Neonatal hypoglycemia, often from hyperinsulinemia, is a significant complication of KS.
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