一名突尼斯患者患有肌萎缩侧索硬化症和多巴反应性肌张力障碍。

IF 3.1 3区 医学 Q2 CLINICAL NEUROLOGY
Imen Kacem, Ikram Sghaier, Hanene Ben Rhouma, Antonia Ratti, Nicola Ticozzi, Vincenzo Silani, Neziha Gouider-Khouja, Riadh Gouider
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引用次数: 0

摘要

多巴反应性肌张力障碍(DRD)是一种常染色体显性遗传病,具有帕金森病和肌张力障碍症状,由影响多巴胺合成的 GCH1 基因致病变体引起。本病例报告首次将多巴反应性肌张力障碍与儿童期发病的渐冻症联系起来,表明北非人群复杂的遗传模式可能导致多种疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Amyotrophic Lateral Sclerosis and Dopa-responsive dystonia in a Tunisian patient
Dopa-responsive dystonia (DRD) is an autosomal dominant disease with parkinsonian and dystonic symptoms caused by GCH1 gene pathogenic variants affecting dopamine synthesis. The present case report is the first to link DRD with childhood-onset with ALS, suggesting that complex inheritance patterns in the North African population may contribute to multiple disorders.
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来源期刊
Parkinsonism & related disorders
Parkinsonism & related disorders 医学-临床神经学
CiteScore
6.20
自引率
4.90%
发文量
292
审稿时长
39 days
期刊介绍: Parkinsonism & Related Disorders publishes the results of basic and clinical research contributing to the understanding, diagnosis and treatment of all neurodegenerative syndromes in which Parkinsonism, Essential Tremor or related movement disorders may be a feature. Regular features will include: Review Articles, Point of View articles, Full-length Articles, Short Communications, Case Reports and Letter to the Editor.
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