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Treatable Ataxia: a comprehensive case series study
  • +10
  • Mahmood reza Ashrafi,
  • Elham Pourbakhtyaran,
  • Mohammad Rohani,
  • Bita Shalbafan,
  • Ali Reza Tavasoli,
  • Sareh Hosseinpour ,
  • Maryam Rasulinezhad ,
  • Zahra Rezaei,
  • Ali Zare Dehnavi ,
  • Seyyed Mohammad Mahdi Hosseiny ,
  • Roya Haghighi,
  • Homa Ghabeli,
  • Morteza Heidari
Mahmood reza Ashrafi
Tehran University of Medical Sciences

Corresponding Author:[email protected]

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Elham Pourbakhtyaran
Tehran University of Medical Sciences
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Mohammad Rohani
Iran University of Medical Sciences
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Bita Shalbafan
Shahid Beheshti University of Medical Sciences
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Ali Reza Tavasoli
Tehran University of Medical Sciences
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Sareh Hosseinpour
Tehran University of Medical Sciences
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Maryam Rasulinezhad
Tehran University of Medical Sciences
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Zahra Rezaei
Tehran University of Medical Sciences
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Ali Zare Dehnavi
Tehran University of Medical Sciences
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Seyyed Mohammad Mahdi Hosseiny
Tehran University of Medical Sciences
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Roya Haghighi
Tehran University of Medical Sciences
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Homa Ghabeli
Tehran University of Medical Sciences
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Morteza Heidari
Tehran University of Medical Sciences
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Abstract

Autosomal recessive cerebellar ataxias are a group of heterogeneous early-onset progressive disorders that some of them are treatable. We performed 4-year-follow up for 25 patients that considered as treatable ataxia in the literature. According to our study, patients would benefit from early detection of treatable ataxia, close observation, and follow-up.
04 Nov 2021Submitted to Clinical Case Reports
18 Nov 2021Submission Checks Completed
18 Nov 2021Assigned to Editor
08 Dec 2021Reviewer(s) Assigned
13 Feb 2022Review(s) Completed, Editorial Evaluation Pending
23 Feb 2022Editorial Decision: Revise Minor
01 Mar 20221st Revision Received
02 Mar 2022Submission Checks Completed
02 Mar 2022Assigned to Editor
02 Mar 2022Review(s) Completed, Editorial Evaluation Pending
28 Mar 2022Editorial Decision: Accept