Community
Early-Onset Ataxia with Oculomotor Apraxia and Hypoalbuminemia
An autosomal recessive cerebellar ataxia that is characterized by progressive cerebellar ataxia including oculomotor apraxia, severe neuropathy and hypoalbuminemia, is caused by autosomal recessive inheritance of mutatio
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 recessive cerebellar ataxia that is characterized by progressive cerebellar ataxia including oculomotor apraxia, severe neuropathy and hypoalbuminemia, is caused by autosomal recessive inheritance of mutatio
Resources
Join the Early-Onset Ataxia with Oculomotor Apraxia and Hypoalbuminemia community
Talk with people who understand, share what helps, and find support from others living with early-onset ataxia with oculomotor apraxia and hypoalbuminemia. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.