Suppr超能文献

与棘红细胞增多症相关的神经学表型。

Neurologic phenotypes associated with acanthocytosis.

作者信息

Walker R H, Jung H H, Dobson-Stone C, Rampoldi L, Sano A, Tison F, Danek A

机构信息

Department of Neurology, James J. Peters Veterans Affairs Medical Center, Bronx, NY 10468, USA.

出版信息

Neurology. 2007 Jan 9;68(2):92-8. doi: 10.1212/01.wnl.0000250356.78092.cc.

Abstract

The term "neuroacanthocytosis" is normally used to refer to autosomal recessive chorea-acanthocytosis and X-linked McLeod syndrome, but there are other movement disorders in which erythrocyte acanthocytosis may also be seen, such as Huntington disease-like 2 and pantothenate kinase-associated neurodegeneration. Disorders of serum lipoproteins such as Bassen-Kornzweig disease form a distinct group of neuroacanthocytosis syndromes in which ataxia is observed, but movement disorders are not seen. Genetic testing has enabled us to distinguish between these disorders, even when there are considerable similarities between phenotypes. Improved detection is important for accurate genetic counseling, for monitoring for complications, and, it is hoped, for implementing causal treatments, once these become available. As in other neurodegenerative conditions, animal models are a promising strategy for the development of such therapies.

摘要

术语“神经棘红细胞增多症”通常用于指常染色体隐性遗传性舞蹈病-棘红细胞增多症和X连锁的麦克劳德综合征,但在其他一些运动障碍中也可能出现红细胞棘形细胞增多,如2型亨廷顿病样综合征和泛酸激酶相关神经变性。血清脂蛋白紊乱,如巴森-科尔兹韦格病,构成了一组独特的神经棘红细胞增多症综合征,其中可观察到共济失调,但未见运动障碍。基因检测使我们能够区分这些疾病,即使它们的表型之间存在相当大的相似性。改进检测对于准确的遗传咨询、监测并发症以及希望在有因果治疗方法时实施这些治疗都很重要。与其他神经退行性疾病一样,动物模型是开发此类疗法的一种有前景的策略。

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