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Successful transition from insulin to sulphonylurea in a child with neonatal diabetes mellitus diagnosed beyond six months of age due to C42R mutation in the KCNJ11 gene
Neonatal diabetes mellitus is a rare monogenic condition affecting 1 in 100,000–300,000 live births. Mutations in the subunits of ATP-sensitive potassium (K(ATP)) channels, which are the central gatekeepers of electrical activity, are the common cause of this condition, thereby reducing insulin secr...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Japanese Society for Pediatric Endocrinology
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297163/ https://www.ncbi.nlm.nih.gov/pubmed/35928374 http://dx.doi.org/10.1297/cpe.2022-0013 |