| Literature DB >> 28664756 |
Elisa Rubino1, Alessandro Vacca1, Salvatore Gallone2, Flora Govone1, Milena Zucca1, Annalisa Gai1, Patrizia Ferrero2, Pierpaola Fenoglio2, Maria Teresa Giordana1,2, Innocenzo Rainero1,2.
Abstract
Bipolar disorder is a chronic psychiatric illness characterised by fluctuation in mood state, with a relapsing and remitting course. Frontotemporal dementia (FTD) is a clinically and genetically heterogeneous syndrome, with the most frequent phenotype being behavioural variant frontotemporal dementia (bvFTD). Here, we report the case of an Italian male presenting with late-onset bipolar disorder that developed into bvFTD over time, carrying a mutation in the GRN gene. Interestingly, the patient carried the c.1639 C > T variant in the GRN gene, resulting in a R547C substitution. Our case report further corroborates the notion that, in addition to FTD, progranulin may be involved in the neurobiology of bipolar disorder type 1, and suggests to screen patients with late-onset bipolar disorder for GRN mutations.Entities:
Keywords: Bipolar disorder type 1; frontotemporal dementia; progranulin gene
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Year: 2017 PMID: 28664756 DOI: 10.1080/21678421.2017.1339716
Source DB: PubMed Journal: Amyotroph Lateral Scler Frontotemporal Degener ISSN: 2167-8421 Impact factor: 4.092