Author:
Ozsu Elif,Giri Dinesh,Seymen Karabulut Gulcan,Senniappan Senthil
Abstract
Abstract
Neonatal diabetes is a rare form of monogenic diabetes characterised by persistent hyperglycaemia during the first 6–9 months of age. About half of the cases of neonatal diabetes are transient forms resulting from mutations in the genes in the imprinted region of chromosome 6q24 and the other half are permanent forms. Activating mutations in the potassium ATP (K
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Reference46 articles.
1. Genetics and pathophysiology of neonatal diabetes mellitus;J Diabetes Investig,2011
2. Novel homozygous likely-pathogenic intronic variant in INS causing permanent neonatal diabetes in siblings;J Pediatr Endocrinol Metab,2016
3. Sulfonylurea in the treatment of neonatal diabetes mellitus children with heterogeneous genetic backgrounds;J Pediatr Endocrinol Metab,2015
4. Neonatal diabetesmellitus-genetic aspects;Pediatr Endocrinol Rev,2004
5. Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11;Nat Clin Pract Neurol,2007
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