Inukai Kouichi, Awata Takuya, Inoue Kiyoaki, Kurihara Susumu, Nakashima Youhei, Watanabe Masaki, Sawa Takahiro, Takata Nobuki, Katayama Shigehiro
Division of Endocrinology and Diabetes, Department of Medicine, Saitama Medical School, Morohongo 38, Moroyama, Iruma-gun, Saitama 350-0495, Japan.
Diabetes Res Clin Pract. 2005 Aug;69(2):136-41. doi: 10.1016/j.diabres.2005.01.002. Epub 2005 Feb 24.
Wolfram syndrome (WFS) is an autosomal recessive disorder characterized by early onset diabetes mellitus, progressive optic atrophy, sensorineural deafness and diabetes insipidus. Affected individuals may also have renal tract abnormalities as well as neurogical and psychiatric syndromes. WFS1 encoding a transmembrane protein was identified as the gene responsible for WFS. We report herein a Japanese family, of which two members had this syndrome. In the WFS1 gene of these patients, we identified a novel mutation, a nine nucleotide insertion (AFF344-345ins). In addition, one of these patients had preclinical hypopituitarism, which is an unusual feature of WFS. As only the two family members homozygous for the mutation showed WFS, these data support the notion that this mutation is the cause of WFS.
沃夫勒姆综合征(WFS)是一种常染色体隐性疾病,其特征为早发性糖尿病、进行性视神经萎缩、感音神经性耳聋和尿崩症。患者还可能有泌尿道异常以及神经和精神综合征。编码跨膜蛋白的WFS1被确定为导致WFS的基因。我们在此报告一个日本家庭,其中两名成员患有这种综合征。在这些患者的WFS1基因中,我们发现了一个新的突变,即九个核苷酸的插入(AFF344 - 345ins)。此外,其中一名患者有临床前垂体功能减退,这是WFS的一个不寻常特征。由于只有两名该突变纯合的家庭成员表现出WFS,这些数据支持了该突变是WFS病因的观点。