25例可治疗性共济失调患者的随访：一项综合病例系列研究。
Follow-up of 25 patients with treatable ataxia: A comprehensive case series study.
作者信息
Ashrafi Mahmoud Reza, Pourbakhtyaran Elham, Rohani Mohammad, Shalbafan Bita, Tavasoli Ali Reza, Hosseinpour Sareh, Rasulinezhad Maryam, Rezaei Zahra, Zare Dehnavi Ali, Hosseiny Seyyed Mohammad Mahdi, Haghighi Roya, Ghabeli Homa, Heidari Morteza
机构信息
Department of Paediatrics Division of Paediatric Neurology, Growth and Development Research Center Children's Medical Centre Paediatrics Centre of Excellence Tehran University of Medical Sciences Tehran Iran.
Department of Neurology School of Medicine Hazrat Rasool-E Akram General Hospital Iran University of Medical Sciences Tehran Iran.
出版信息
Clin Case Rep. 2022 Apr 20;10(4):e05777. doi: 10.1002/ccr3.5777. eCollection 2022 Apr.
Autosomal recessive cerebellar ataxias are a group of heterogeneous early-onset progressive disorders that some of them are treatable. We performed a 4-year follow-up for 25 patients who had treatable ataxia. According to our study, patients would benefit from early detection of treatable ataxia, close observation, and follow-up.
常染色体隐性遗传性小脑共济失调是一组异质性早发性进行性疾病，其中一些是可治疗的。我们对25例可治疗性共济失调患者进行了4年的随访。根据我们的研究，患者将从可治疗性共济失调的早期发现、密切观察和随访中获益。
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