上海交通大学学报(医学版) ›› 2017, Vol. 37 ›› Issue (6): 881-.doi: 10.3969/j.issn.1674-8115.2017.06.029

• 病例报告 • 上一篇    

新发现#br# TSC1#br# 基因杂合错义突变 c.T1967C 致结节性硬化症的 1 例散发病例

姚梦莎 1,刘军 2   

  1. 1. 上海交通大学 医学院,上海 200025;2. 上海交通大学 医学院附属瑞金医院神经内科,上海 200025
  • 出版日期:2017-06-28 发布日期:2017-07-05
  • 通讯作者: 刘军,电子信箱:jly0520@hotmail.com
  • 作者简介:?姚梦莎(1992—),女,博士生;电子信箱:may-1123@163.com
  • 基金资助:

    上海市教育委员会高峰高原学科建设计划(20152201)

A sporadic case of tuberous sclerosis complex caused by a newly found heterozygous missense mutation of c.T1967C in TSC1 gene

YAO Meng-sha1, LIU Jun2   

  1. 1. Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China; 2. Department of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China
  • Online:2017-06-28 Published:2017-07-05
  • Supported by:

     Shanghai Municipal Education Commission—Gaofeng Clinical Medicine Grant Support, 20152201

摘要:

报道 1 例通过第 2 代高通量基因检测技术诊断为结节性硬化症的 29 岁中国汉族女性散发病例。该患者因反复癫痫发作 26 年, 头晕头痛 3 个月入院;查体可见面部弥漫性血管纤维瘤、腰背部散在鲨鱼皮样斑块、躯干四肢散在色素减退斑片;头颅磁共振见病灶 累及侧脑室、小脑蚓部、左侧颞叶,伴两侧广泛脑皮质异常信号改变。基因测序发现该患者 TSC1 基因 16 号外显子 c.T1967C 杂合错 义突变,且此突变位点为一新发现致病性突变位点。

关键词: 结节性硬化症, TSC1 基因, 错义突变, 散发

Abstract:

 This paper reported a sporadic case of a 29-year-old Han female diagnosed with tuberous sclerosis complex (TSC) by next generation sequencing (NGS), one of genetic analysis techniques. She was admitted because of recurrent intractable seizure for 26 years, dizziness and headache for 3 months. Physical examination revealed angiofibromas over her face, shagreen patches in her lower back area, and hypomelanotic macules around her limbs and body. Cranial MRI manifested lesions on lateral ventricles, cerebellar vermis and left temporal lobe with abnormal signal changes on both sides of extensive cerebral cortex. A pathogenic and heterozygous missense mutation, c.T1967C, in exon 16 of her TSC1 gene was found via genetic tests, which has not yet been reported before.

Key words: tuberous sclerosis complex, TSC1 gene, missense mutation, sporadic