Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family

Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family

Introduction: Inclusion body myopathy with Paget's disease of the bone and frontotemporal dementia (IBMPFD) is a rare late-onset autosomal dominant disorder due to a mutation of the valosin-containing protein (VCP) gene. Case Report: We report the case of a patient who developed progressive wea...

Full description

Bibliographic Details
Main Authors: Agnès Jacquin, Olivier Rouaud, Pierre Soichot, Yannick Bejot, Inna Dygai-Cochet, Marie Sarazin, Tania Stojkovic, Martine Lemesle-Martin, Maurice Giroud, Thibault Moreau
Format: Article
Language:English
Published: Karger Publishers 2013-10-01
Series:Case Reports in Neurology
Subjects:
Frontotemporal dementia
Inclusion body myopathy
VCP mutation
Psychiatric disorders
Online Access:http://www.karger.com/Article/FullText/356481

Internet

http://www.karger.com/Article/FullText/356481

Similar Items