Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study.

Autor:	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
Předmět:	ATAXIA SPINOCEREBELLAR ataxia CEREBELLUM degeneration
Zdroj:	Clinical Case Reports; Apr2022, Vol. 10 Issue 4, p1-6, 6p
Abstrakt:	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. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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