Suppr超能文献

多巴反应性肌张力障碍:共济失调毛细血管扩张症的早期表现。

Dopa-Responsive Dystonia: An Early Presentation of Ataxia-Telangiectasia.

作者信息

Arora Anshita, Bajaj Shruti, Rathod Nishant, Hegde Anaita U

机构信息

DNB Pediatrics, Fellowship in Pediatric Neurology, Clinical Associate in Pediatric Neurology, Jaslok Hospital and Research Center, Mumbai, Maharashtra, India.

MD Pediatrics, Fellowship in Clinical Genetics (MUHS), Consultant Clinical Geneticist, NH SRCC Children Hospital, Mumbai, Maharashtra, India.

出版信息

Ann Indian Acad Neurol. 2022 Nov-Dec;25(6):1167-1169. doi: 10.4103/aian.aian_690_22. Epub 2022 Nov 23.

Abstract

Ataxia-telangiectasia (AT) is a complex genetic neurodegenerative disease with autosomal recessive inheritance. The typical initial features of ataxia telangiectasia include ataxia, cutaneous telangiectasia, and immune deficiency with recurrent infections. Usually, movement disorder occurs late in the course of the disease. A diagnosis of variant or atypical ataxia-telangiectasia (variant AT) is considered in case of any deviation from the normal course of illness giving rise to variable presentations of the disease. Only a few cases of variant AT with predominant movement disorder have been reported worldwide. A knowledge of atypical presentations helps in early diagnosis and thus to initiate management and counselling of the family at the earliest. Here, we report a case of genetically confirmed ataxia-telangiectasia with an initial presentation of dopamine responsive dystonia.

摘要

共济失调毛细血管扩张症(AT)是一种具有常染色体隐性遗传的复杂遗传性神经退行性疾病。共济失调毛细血管扩张症的典型初始特征包括共济失调、皮肤毛细血管扩张以及伴有反复感染的免疫缺陷。通常,运动障碍在疾病进程后期出现。如果疾病进程偏离正常情况导致出现多种不同表现,则考虑诊断为变异型或非典型共济失调毛细血管扩张症(变异型AT)。全球仅报道了少数以运动障碍为主的变异型AT病例。了解非典型表现有助于早期诊断,从而尽早对家庭开展管理和咨询。在此,我们报告一例基因确诊的共济失调毛细血管扩张症,其初始表现为多巴胺反应性肌张力障碍。

相似文献

本文引用的文献

3
Ataxia telangiectasia: a review.共济失调毛细血管扩张症:综述
Orphanet J Rare Dis. 2016 Nov 25;11(1):159. doi: 10.1186/s13023-016-0543-7.
8
Familial dopa-responsive cervical dystonia.家族性多巴反应性颈部肌张力障碍。
Neurology. 2006 Feb 28;66(4):599-601. doi: 10.1212/01.wnl.0000198501.61063.66.

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