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Ataxia-Oculomotor Apraxia 3
An autosomal recessive cerebellar ataxia that is characterized by poor coordination and balance (ataxia) that worsen over time and that is caused by homozygous mutation in the PIK3R5 gene on chromosome 17p13.
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
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Overview
An autosomal recessive cerebellar ataxia that is characterized by poor coordination and balance (ataxia) that worsen over time and that is caused by homozygous mutation in the PIK3R5 gene on chromosome 17p13.
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