Suppr超能文献

线粒体脑肌病、乳酸酸中毒和卒中样发作综合征(MELAS)的一个扩展家系中不典型症状的家族性复发。

Familial recurrence of atypical symptoms in an extended pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).

作者信息

Dougherty F E, Ernst S G, Aprille J R

机构信息

Division of Genetics and Metabolism, Children's Hospital of Boston, Massachusetts 02115.

出版信息

J Pediatr. 1994 Nov;125(5 Pt 1):758-61. doi: 10.1016/s0022-3476(94)70073-7.

Abstract

We report a clinically heterogeneous, multigenerational pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with a mutation at nucleotide 3243 in the mitochondrial DNA tRNA(Leu)(UUR) gene. Our findings suggest that the mutation at nucleotide 3243 is not always associated with the classic MELAS phenotype and that other symptoms (notably cardiac and gastrointestinal abnormalities) should raise the suspicion of a mitochondrial disorder.

摘要

我们报告了一个临床异质性的多代家系,其患有与线粒体DNA亮氨酰tRNA(UUR)基因第3243位核苷酸突变相关的线粒体脑肌病、乳酸酸中毒和卒中样发作综合征(MELAS)。我们的研究结果表明,第3243位核苷酸的突变并不总是与经典的MELAS表型相关,其他症状(尤其是心脏和胃肠道异常)应引起对线粒体疾病的怀疑。

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