Catalog

Frontotemporal dementia due to CHMP2B mutation

No MMS code

Link to WHO Definition

Frontotemporal dementia due to CHMP2B mutation – http://id.who.int/icd/entity/1752271020

A rare genetic FTD due to a mutation in the gene encoding charged multivesicular body protein 2B on chromosome 3. It can present as a behavioural syndrome. It can also be associated with motor neuron disease.