Myotonic dystrophy type 1 (DM1) is an autosomal dominant disorder caused by an unstable CTG-repeat expansion in the DM1 protein kinase gene (DMPK gene) on chromosome 19q13.3 [1]. The disorder is multi-systemic with symptoms from the muscles, eyes, heart, brain, gastrointestinal tract and endocrine system [2,3].

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