A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations

A. K. Ovsyannikova, O. D. Rymar, D. E. Ivanoshchuk, Svetlana V. Mikhailova, E. V. Shakhtshneider, P. S. Orlov, E. S. Malakhina, M. I. Voevoda

Результат исследования: Научные публикации в периодических изданияхстатьярецензирование

3 Цитирования (Scopus)

Аннотация

Diabetes mellitus with autosomal dominant inheritance, i.e., maturity-onset diabetes of the young (MODY), is a genetic form of diabetes mellitus. The MODY phenotype is associated with gene mutations leading to pancreatic β-cell dysfunction. Here, we present the clinical case of a 50-year-old proband with familial diabetes mellitus in five generations (proband, her mother, grandmother, great-grandfather, and son). This disease is most likely associated with the novel Ser6Arg mutation in the HNF1A gene, which was identified in four family members. The mutation was not detected in MODY patients (126 subjects), in patients with type 2 diabetes mellitus (188 subjects), and in a general population sample (564 subjects).

Язык оригиналаанглийский
Страницы (с-по)413-420
Число страниц8
ЖурналDiabetes Therapy
Том9
Номер выпуска1
DOI
СостояниеОпубликовано - 1 фев 2018

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