Suppr超能文献

L1综合征患者的临床和遗传特征:两种新突变的定义

Clinical and genetic features of L1 syndrome patients: Definition of two novel mutations.

作者信息

Isik Esra, Onay Huseyin, Atik Tahir, Akgun Bilcag, Cogulu Ozgur, Ozkinay Ferda

机构信息

Subdivision of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey.

Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.

出版信息

Clin Neurol Neurosurg. 2018 Sep;172:20-23. doi: 10.1016/j.clineuro.2018.06.007. Epub 2018 Jun 18.

Abstract

L1 syndrome is a rare X linked recessive disorder caused bygene mutations in the L1 cell adhesion molecule (L1CAM), and characterized by hydrocephalus, intellectual disability, adducted thumbs and spasticity of the legs. The gene encodes a protein which plays an important role in neuronal development. Two unrelated L1 syndrome cases, with global developmental delay and hydrocephalus, were referred to pediatric genetics subdivision for genetic counseling. Bilateral adducted thumbs and spasticity in the lower extremities were also observed in both patients. Molecular analysis revealed two novel hemizygous mutations in the patients: a deletion mutation (c.749delG; p.Ser250Thrfs*51) and a splicing mutation (c.3166+1G>A). To conclude; in male patients with intellectual disability and hydrocephalus, where adducted thumbs are present, L1 syndrome should be considered.

摘要

L1综合征是一种罕见的X连锁隐性疾病,由L1细胞粘附分子(L1CAM)基因突变引起,其特征为脑积水、智力障碍、拇指内收和腿部痉挛。该基因编码一种在神经元发育中起重要作用的蛋白质。两名无亲缘关系的L1综合征病例,伴有全面发育迟缓及脑积水,被转诊至儿科遗传学部门进行遗传咨询。两名患者均观察到双侧拇指内收及下肢痉挛。分子分析显示患者存在两个新的半合子突变:一个缺失突变(c.749delG;p.Ser250Thrfs*51)和一个剪接突变(c.3166+1G>A)。总之,对于存在拇指内收的智力障碍和脑积水男性患者,应考虑L1综合征。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验