Cerebral involvement and related aspects in myotonic dystrophy type 2
Abstract
Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder caused by CCTG repeats expansion in the first intron of the CNBP gene. In this review we focus on the brain involvement in DM2, including its pathogenic mechanisms, microstructural, macrostructural and functional brain changes, as well as the effects of all these impairments on patients' everyday life. We also try to understand how brain abnormalities in DM2 should...
Paper Details
Title
Cerebral involvement and related aspects in myotonic dystrophy type 2
Published Date
Aug 1, 2021
Journal
Volume
31
Issue
8
Pages
681 - 694
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