Spinocerebellar ataxia (SCA) presents a formidable challenge for patients and families alike. This progressive disorder influences coordination, balance, and speech, gradually eroding quality of life. While there is currently no treatment for SCA, a spectrum of treatment approaches are available to alleviate symptoms and improve overall well-being.
although the multifactorial presentation of the ataxic affected individual might look overwhelmingly complex, making use of any in the numerous out there therapeutic interventions for the individual symptom areas can often assist [six]. MSA-C progresses considerably more swiftly than ILOCA and genetic ataxia and causes substantial disability in a
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