Successful transfer from insulin to oral sulfonylurea in a 3-year-old girl with a mutation in the KCNJ11 gene

Neonatal diabetes mellitus is considered a rare disease that is diagnosed in the first six months of life, and can be either transient or permanent. Recent advances in molecular genetics have shown that activating mutations in KCNJ11 (the gene that encodes for the Kir6.2 subunit of the K(ATP) potass...

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Detalles Bibliográficos
Autores principales: Al-Mahdi, Maria, Al Mutair, Angham, Al Balwi, Mohammed, Hussain, Khalid
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855071/
https://www.ncbi.nlm.nih.gov/pubmed/20220270
http://dx.doi.org/10.4103/0256-4947.60526

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855071/
https://www.ncbi.nlm.nih.gov/pubmed/20220270
http://dx.doi.org/10.4103/0256-4947.60526

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