Community
Cerebellar Ataxia Type 48
An autosomal dominant cerebellar ataxia characterized by mid-adult onset of gait ataxia and/or cognitive-affective symptoms that is caused by heterozygous mutation in the STUB1 gene on chromosome 16p13.3.
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 autosomal dominant cerebellar ataxia characterized by mid-adult onset of gait ataxia and/or cognitive-affective symptoms that is caused by heterozygous mutation in the STUB1 gene on chromosome 16p13.3.
Resources
Join the Cerebellar Ataxia Type 48 community
Talk with people who understand, share what helps, and find support from others living with cerebellar ataxia type 48. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.