Open AccessFollow‐up of 25 patients with treatable ataxia: A comprehensive case series study
Author(s) -
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
Publication year - 2022
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.5777
Subject(s) - medicine , series (stratigraphy) , ataxia , pediatrics , intensive care medicine , general surgery , psychiatry , paleontology , biology
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.