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Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia
A syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and is caused by mutation in the valosin containing protein.
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
A syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and is caused by mutation in the valosin containing protein.
Resources
Join the Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia community
Talk with people who understand, share what helps, and find support from others living with inclusion body myopathy with paget disease of bone and frontotemporal dementia. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.