Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene

Monogenic diabetes caused by mutations in the glucokinase gene (GCK-MODY) is usually characterized by a mild clinical phenotype. The clinical course of diabetes may be, however, highly variable. The authors present a child with diabetes manifesting with ketoacidosis during the neonatal period, born...

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Detalles Bibliográficos
Autores principales: Borowiec, Maciej, Mysliwiec, Malgorzata, Fendler, Wojciech, Antosik, Karolina, Brandt, Agnieszka, Malecki, Maciej, Mlynarski, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162147/
https://www.ncbi.nlm.nih.gov/pubmed/21437567
http://dx.doi.org/10.1007/s00592-011-0279-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162147/
https://www.ncbi.nlm.nih.gov/pubmed/21437567
http://dx.doi.org/10.1007/s00592-011-0279-8

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