Schizophrenia syndrome due to C9ORF72 mutation case report: a cautionary tale and role of hybrid brain imaging!

BACKGROUND: Frontal variant frontotemporal dementia is a common cause of presenile dementia. A hexanucleotide expansion on chromosome 9 has recently been recognized as the most common genetic mutation cause of this illness. This sub-type tends to present psychiatrically with psychosis being a common...

Descripción completa

Detalles Bibliográficos
Autores principales: Burhan, A. M., Anazodo, U. C., Marlatt, N. M., Palaniyappan, L., Blair, M., Finger, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254365/
https://www.ncbi.nlm.nih.gov/pubmed/34217252
http://dx.doi.org/10.1186/s12888-021-03341-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254365/
https://www.ncbi.nlm.nih.gov/pubmed/34217252
http://dx.doi.org/10.1186/s12888-021-03341-9

Ejemplares similares