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ABSTRACT: Background
The overlap between frontotemporal dementia (FTD) and primary psychiatric disorders has been brought to light by reports of prominent neuropsychiatric symptoms (NPS) in FTD-related genetic mutations, particularly among C9orf72 and GRN carriers. It has been recently demonstrated that early neuroanatomical changes in genetic FTD may be different across the major disease-causing mutations.Objective
We aimed to identify whether NPS could be driven by distinct structural correlates.Methods
One hundred and sixty-seven mutation carriers (75 GRN, 60 C9orf72, and 32 MAPT) were included from the Genetic FTD Initiative (GENFI) study, a large international cohort of genetic FTD. Neuropsychiatric symptoms including delusions, hallucinations (visual, auditory, and tact
SUBMITTER: Sellami L
PROVIDER: S-EPMC6087430 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature