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- Title
Mutant Neurogenin-3 in Permanent Neonatal Diabetes and Congenital Malabsorptive Diarrhea.
- Authors
Hancili, Suna; Guven, Ayla; Vaxillaire, Martine
- Abstract
The article presents a case study of a 20-month-old male patient with hyperglycemia. The patient has no history of diabetes in the parents or relatives but had suffered from non-progressive non-ketotic moderate hyperglycemia. The article also revealed that a recessive null mutation in neurogenin 3 (NEUROG3) may cause a rare form of neonatal diabetes with congenital malabsorptive diarrhea.
- Subjects
HYPERGLYCEMIA; NEUROGENIN 3; NEUROGENINS; DIABETES in children; PEDIATRIC endocrinology
- Publication
Journal of Clinical Research in Pediatric Endocrinology, 2015, Vol 7, p10
- ISSN
1308-5727
- Publication type
Case Study