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Updated: Jun 25, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
Myotonic dystrophy type 2 with focal asymmetric muscle weakness and no electrical myotonia
Margherita Milone1, Sat D Batish, Jasper R Daube
1Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, Minnesota, 55905, USA. Milone.Margherita@mayo.edu
Abstract:
Genetically proven myotonic dystrophy type 2 (DM2) was found in a 61-year-old woman with creatine kinase (CK) elevation and only isolated weakness of one triceps. There was no clinical or electrical myotonia. Electromyography (EMG) showed only scattered fibrillation potentials and short duration motor unit potentials. Muscle biopsy showed nonspecific myopathic features and highly atrophic fibers with nuclear clumps. DM2 should be considered in patients with focal proximal weakness and abnormal EMG without myotonic discharges.
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