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Spastic Ataxia 5
A spastic ataxia that is characterized by early onset of cerebellar ataxia, spasticity, oculomotor apraxia, dystonia and myoclonic epilepsy, is caused by homozygous mutation in the AFG3L2 gene on chromosome 18p11.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
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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
A spastic ataxia that is characterized by early onset of cerebellar ataxia, spasticity, oculomotor apraxia, dystonia and myoclonic epilepsy, is caused by homozygous mutation in the AFG3L2 gene on chromosome 18p11.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.