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X-Linked Spinocerebellar Ataxia 5
An X-linked cerebellar ataxia characterized by neonatal hypotonia, delayed motor development, nonprogressive ataxia, nystagmus, and dysarthria that is caused by hemizygous mutation in region of chromosome Xq25-q27.1.
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.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
An X-linked cerebellar ataxia characterized by neonatal hypotonia, delayed motor development, nonprogressive ataxia, nystagmus, and dysarthria that is caused by hemizygous mutation in region of chromosome Xq25-q27.1.
Resources
Join the X-Linked Spinocerebellar Ataxia 5 community
Talk with people who understand, share what helps, and find support from others living with x-linked spinocerebellar ataxia 5. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.