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...

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Detalles Bibliográficos
Autores principales: Jacquin, Agnès, Rouaud, Olivier, Soichot, Pierre, Bejot, Yannick, Dygai-Cochet, Inna, Sarazin, Marie, Stojkovic, Tania, Lemesle-Martin, Martine, Giroud, Maurice, Moreau, Thibault
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Published online: October, 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843933/
https://www.ncbi.nlm.nih.gov/pubmed/24348398
http://dx.doi.org/10.1159/000356481

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843933/
https://www.ncbi.nlm.nih.gov/pubmed/24348398
http://dx.doi.org/10.1159/000356481

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