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一名莱施-奈恩病患者的左旋多巴治疗:病理学、生物化学、神经影像学及治疗相关论述

Levodopa therapy in a Lesch-Nyhan disease patient: pathological, biochemical, neuroimaging, and therapeutic remarks.

作者信息

Serrano Mercedes, Pérez-Dueñas Belen, Ormazábal Aida, Artuch Rafael, Campistol Jaume, Torres Rosa J, García-Cazorla Angels

机构信息

Neurology Department, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.

出版信息

Mov Disord. 2008 Jul 15;23(9):1297-300. doi: 10.1002/mds.21786.

Abstract

Lesch-Nyhan disease (LND) is a hereditary disorder of purine metabolism causing severe neurobehavioral disturbances in which an abnormal central nervous system dopaminergic function has been implied. However, levodopa treatment has rarely been used, and reports describe heterogeneous responses. We report an LND patient with low dopamine metabolite values in cerebrospinal fluid for whom early levodopa/carbidopa therapy was begun with a notable clinical improvement. We propose that very early treatment of LND patients with levodopa may improve their neurological symptoms and may contribute to a better outcome.

摘要

莱施-奈恩病(LND)是一种嘌呤代谢的遗传性疾病,可导致严重的神经行为障碍,其中中枢神经系统多巴胺能功能异常已被提及。然而,左旋多巴治疗很少被使用,且报告描述的反应各异。我们报告了一名脑脊液中多巴胺代谢产物值较低的LND患者,对其早期开始使用左旋多巴/卡比多巴治疗后临床有显著改善。我们提出,对LND患者尽早使用左旋多巴治疗可能会改善其神经症状,并可能有助于获得更好的结果。

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