Health-related quality of life, pain, and fatigue in myotonic dystrophy type 2: a 13-year follow-up study

HRQoL decreased over 13 years in DM2. Pain was present early in the DM2 disease course and did not increase significantly. Healthcare professionals should be aware of the long-term impact of myotonic dystrophy (DM) on pain, fatigue, physical and mental functioning, including social functioning. Symptomatic treatment of these aspects may decrease disease impact, because DM cannot be cured.

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Publication Details

Journal
Disability and Rehabilitation
Published
2025-10-31
DOI
https://doi.org/10.1080/09638288.2025.2571068
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
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article

Health-related quality of life, pain, and fatigue in myotonic dystrophy type 2: a 13-year follow-up study

Nicol Cornelia Voermans, Karlien Mul, Baziel G.M. van Engelen, Alide A. Tieleman et al.
Disability and Rehabilitation
Genetic Neurodegenerative Diseases
article

Health-related quality of life, pain, and fatigue in myotonic dystrophy type 2: a 13-year follow-up study

Nicol Cornelia Voermans, Karlien Mul, Baziel G.M. van Engelen, Alide A. Tieleman, M. Damen
article en

Abstract

HRQoL decreased over 13 years in DM2. Pain was present early in the DM2 disease course and did not increase significantly. Healthcare professionals should be aware of the long-term impact of myotonic dystrophy (DM) on pain, fatigue, physical and mental functioning, including social functioning. Symptomatic treatment of these aspects may decrease disease impact, because DM cannot be cured.

Disability and Rehabilitation
Radboud University Nijmegen (NL), Medisch Spectrum Twente (NL), University Medical Center (US), Radboud University Medical Center (NL)
Openalex Percentile: Top 65%
Genetic Neurodegenerative Diseases
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