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Aim
Myotonic dystrophy type 1 (DM1), a neuromuscular disorder, is divided into four clinical phenotypes: congenital; childhood; adult‐onset, and late‐onset. Publications about the childhood phenotype, especially the long‐term outcome, are scarce. The aims of this study were to assess and describe participation outcomes in adults with the childhood phenotype.
Method
A retrospective chart methodology...
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