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Spinocerebellar Ataxia 25
An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, is caused by repeat CAG expansion on chromosome 2p15-p21.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, is caused by repeat CAG expansion on chromosome 2p15-p21.
Resources
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