| Literature DB >> 32279720 |
Kimberly Tsu Kwei1, Sheng-Han Kuo2.
Abstract
Cerebellar ataxia can be caused by a variety of disorders, including degenerative processes, autoimmune and paraneoplastic illness as well as by gene mutations inherited in autosomal dominant, autosomal recessive, or X-linked fashions. In this review, we highlight the treatments for cerebellar ataxia in a systematic way, to provide guidance for clinicians who treat patients with cerebellar ataxia. In addition, we review therapies currently under development for ataxia, which we feel is currently one of the most exciting fields in neurology.Entities:
Keywords: Ataxia; Ataxia treatment; Cerebellum; Friedreich ataxia; Multiple system atrophy; Spinocerebellar ataxia
Mesh:
Year: 2020 PMID: 32279720 PMCID: PMC7220524 DOI: 10.1016/j.ncl.2020.01.008
Source DB: PubMed Journal: Neurol Clin ISSN: 0733-8619 Impact factor: 3.806