Cortical Frontoparietal Network Dysfunction in CHMP2B-Frontotemporal Dementia

Cortical Frontoparietal Network Dysfunction in CHMP2B-Frontotemporal Dementia

A rare cause of inherited frontotemporal dementia (FTD) is a mutation in the CHMP2B gene on chromosome 3 leading to the autosomal dominantly inherited FTD (CHMP2B-FTD). Since CHMP2B-FTD is clinically well-characterized, and patients show a distinct pattern of executive dysfunction, the condition off...

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Bibliographic Details
Main Authors: Christian Sandøe Musaeus, Jette Stokholm Pedersen, Troels Wesenberg Kjær, Peter Johannsen, Gunhild Waldemar, Maria Joy Normann Haverberg, Theis Bacher, Jørgen Erik Nielsen, Peter Roos, The FReJA Consortium, S Gydesen, J Brown, AM Isaacs, J Collinge, A Gade, E Englund, E Fisher, TT Nielsen, T Thusgaard, I Holm
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Aging Neuroscience
Subjects:
EEG
microstates
spectral power
FTD
Frontotemporal dementia
CHMP2B
Online Access:https://www.frontiersin.org/articles/10.3389/fnagi.2021.714220/full

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