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...

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Detalles Bibliográficos
Autores principales: Poon, Sarah Wing-yiu, Chung, Brian Hon-yin, Tsang, Mandy Ho-yin, Tung, Joanna Yuet-ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2022
Materias:
Case Report
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

Internet

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

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