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


ABSTRACT: 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.

SUBMITTER: Watson A 

PROVIDER: S-EPMC4724461 | biostudies-literature | 2016 Jan

REPOSITORIES: biostudies-literature

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

Watson Annie A   Pribadi Mochtar M   Chowdari Kodavali K   Clifton Sue S   Joel Wood   Miller Bruce L BL   Coppola Giovanni G   Nimgaonkar Vishwajit V  

Psychiatry research 20151208


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  ...[more]

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