Advances In Spinocerebellar Ataxia Research: Current Breakthroughs and Future Directions
Received Date: May 01, 2024 / Published Date: May 31, 2024
Abstract
Spinocerebellar ataxia (SCA) refers to a group of inherited neurodegenerative disorders characterized by progressive loss of coordination, balance, and motor function. Affecting the cerebellum and spinal cord, SCAs are caused by genetic mutations, and their symptoms typically worsen over time, impacting a patient’s quality of life. To date, more than 40 different types of SCAs have been identified, each associated with specific genetic mutations. Despite the complexity and genetic variability of the disorder, recent advances in research are shedding light on its underlying mechanisms and offering hope for the development of effective treatments [1]. This article will explore the latest breakthroughs in SCA research and examine potential future direction
Citation: Lukas SE (2024) Advances In Spinocerebellar Ataxia Research: CurrentBreakthroughs and Future Directions. J Clin Exp Neuroimmunol, 9: 238.
Copyright: © 2024 Lukas SE. This is an open-access article distributed under theterms of the Creative Commons Attribution License, which permits unrestricteduse, distribution, and reproduction in any medium, provided the original author andsource are credited.
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