Article
Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations.
Journal of neurology - 1 Aug 2022
Bouzigues Arabella, Russell Lucy L, Peakman Georgia, Bocchetta Martina, Greaves Caroline V, Convery Rhian S, Todd Emily, Rowe James B, Borroni Barbara, Galimberti Daniela, Tiraboschi Pietro, Masellis Mario, Tartaglia Maria Carmela, Finger Elizabeth, van Swieten John C, Seelaar Harro, Jiskoot Lize, Sorbi Sandro, Butler Chris R, Graff Caroline, Gerhard Alexander, Langheinrich Tobias, Laforce Robert, Sanchez-Valle Raquel, de Mendonça Alexandre, Moreno Fermin, Synofzik Matthis, Vandenberghe Rik, Ducharme Simon, Le Ber Isabelle, Levin Johannes, Danek Adrian, Otto Markus, Pasquier Florence, Santana Isabel, Rohrer Jonathan D
Abstract excerpt
INTRODUCTION: A third of frontotemporal dementia (FTD) is caused by an autosomal-dominant genetic mutation in one of three genes: microtubule-associated protein tau (MAPT), chromosome 9 open reading frame 72 (C9orf72) and progranulin (GRN). Prior studies of prodromal FTD have identified impaired executive function and social cognition early in the disease but few have studied naming in detail. METHODS: We...
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