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 has_material_basis_in mutation in the valosin containing protein.

Also known as: IBMPFD; inclusion body myopathy with Paget's disease of bone and frontotemporal dementia