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Autosomal Recessive Spinocerebellar Ataxia 23
An autosomal recessive cerebellar ataxia characterized by epilepsy, intellectual disability, and gait ataxia that is caused by homozygous or compound heterozygous mutation in the TDP2 gene on chromosome 6p22.3.
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.
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Overview
An autosomal recessive cerebellar ataxia characterized by epilepsy, intellectual disability, and gait ataxia that is caused by homozygous or compound heterozygous mutation in the TDP2 gene on chromosome 6p22.3.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.