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Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dement
An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that is caused by heterozygous mutation in VCP on chromosome 9p13.3.
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 inclusion body myopathy with Paget disease of bone and frontotemporal dementia that is caused by heterozygous mutation in VCP on chromosome 9p13.3.
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Talk with people who understand, share what helps, and find support from others living with inclusion body myopathy with early-onset paget disease of bone with or without frontotemporal dement. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.