Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Abstract: We identified in a cohort of patients with frontotemporal dementia (n = 481) or amyotrophic lateral sclerosis (n = 147), 10 index patients carrying a TBK1 loss of function mutation reducing TBK1 expression by 50%. Here, we describe the clinical and pathological characteristics of the 10 index patients and six of their affected relatives carrying a TBK1 mutation. Six TBK1 carriers were diagnosed with frontotemporal dementia, seven with amyotrophic lateral sclerosis, one with both clinical phenotypes and two with dementia unspecified. The mean age at onset of all 16 TBK1 carriers was 6... Mehr ...

Verfasser: Van Mossevelde, Sara
van der Zee, Julie
Gijselinck, Ilse
Engelborghs, Sebastiaan
Sieben, Anne
Van Langenhove
Baets, Jonathan
Ceyssens, Sarah
Van den Broeck, Marleen
Peeters, Karin
Mattheijssens, Maria
Cras, Patrick
De Jonghe, Peter
Martin, Jean-Jacques
De Deyn, Peter Paul
Cruts, Marc
Van Broeckhoven, Christine
Dokumenttyp: Artikel
Erscheinungsdatum: 2016
Schlagwörter: Biology / Human medicine
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26527278
Datenquelle: BASE; Originalkatalog
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Link(s) : https://hdl.handle.net/10067/1299280151162165141