Catalog

Frontotemporal dementia due to VCP mutation

No MMS code

Link to WHO Definition

Frontotemporal dementia due to VCP mutation – http://id.who.int/icd/entity/1650171830

FTD due to mutations in the valosin-containing protein on chromosome 9. It is also associated with inclusion body myositis and Paget's disease of the bone, as well as motor neuron disease. Neuropathologically there are ubiquitin positive inclusions

Parents