C9orf72 repeat expansions that cause frontotemporal dementia are detectable among patients with psychosis.

Psychiatry Res

Department of Psychiatry, University of Pittsburgh, School of Medicine, Pittsburgh, PA, United States; Department of Human Genetics, University of Pittsburgh, Graduate School of Public Health, Pittsburgh, PA, United States. Electronic address:

Published: January 2016

A pathologic hexanucleotide repeat expansion in C9orf72 causes frontotemporal dementia (FTD) or amyotrophic lateral sclerosis (ALS). Behavioral abnormalities can also occur among mutation carriers with FTD, but it is uncertain whether such mutations occur among persons with psychoses per se. Among participants in a genetic study of psychoses (N=739), two pairs of related individuals had C9orf72 expansions, of whom three were diagnosed with schizophrenia (SZ) / schizoaffective disorder (SZA), but their clinical features did not suggest dementia or ALS. A few patients with SZ/SZA carry C9orf72 repeat expansions; such individuals are highly likely to develop FTD/ALS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724461PMC
http://dx.doi.org/10.1016/j.psychres.2015.12.007DOI Listing

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