[A novel mutation W257R in GCK gene discovered from a Chinese patient with maturity onset diabetes of the young]

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Apr 25;48(2):200-203. doi: 10.3785/j.issn.1008-9292.2019.04.12.
[Article in Chinese]

Abstract

Maturity onset diabetes of the young (MODY) is a monogenic autosomal dominant inherited disease. Its clinical manifestations are asymptomatic with slightly elevated fasting blood glucose and few complications. This paper reports a novel mutation W257R in glucokinase (GCK) gene from a Chinese patient with MODY. Heterozygous mutation c.769T>C (p.W257R) in exon 7 of GCK gene (Chr744187343) was found in the proband, her father and brother. This W257R mutation was first reported in Chinese population.

青少年发病的成人型糖尿病(MODY)是一类以常染色体显性模式遗传的单基因疾病,临床表现以无症状、轻度空腹血糖升高为特征,很少出现糖尿病并发症。本文报道一例中国人群中葡萄糖激酶( GCK)基因新发W257R突变所致的MODY。在先证者及父亲、弟弟中均发现GCK基因(Chr744187343)第7号外显子的杂合突变c.769T>C(p.W257R)。该家系中W257R突变在中国人群中为首发。

Publication types

  • Case Reports

MeSH terms

  • China
  • Diabetes Mellitus, Type 2* / genetics
  • Female
  • Glucokinase* / genetics
  • Humans
  • Male
  • Mutation*
  • Pedigree

Substances

  • Glucokinase

Supplementary concepts

  • Mason-Type Diabetes