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- W2337757760 abstract "The clinical relevance and extent of cognitive impairment in adult myotonic dystrophy type 1 (DM1) and 2 (DM2) is still unclear. The aim of this study was to deter- mine whether previously reported cognitive abnormalities progress over time and if this occurs in DM2 as it does in DM1. Fifty-six patients with DM1 and 29 patients with DM2 were subjected to muscle strength assessment, and to a complete battery of neuropsychological tests. Repeated assessment was performed in 20 DM1 and 13 DM2 over time (DM1 mean follow-up: 7.3±2.7 years; DM2 mean fol- low-up: 9.5±2.4 years). Muscle strength and test scores for frontal lobe functions worsened significantly over time (p<0.01), in both DM1 and DM2. DM2 is a progressive muscle disorder, although less severe than DM1. In both DM1 and DM2 frontal cognitive impairment (attentional)" @default.
- W2337757760 created "2016-06-24" @default.
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- W2337757760 date "2007-01-01" @default.
- W2337757760 modified "2023-09-27" @default.
- W2337757760 title "V. SansoneS. GandossiniM. CotelliM. CalabriaO. ZanettiG. Meola Cognitive impairment in adult myotonic dystrophies: a longitudinal study" @default.
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