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Updated: Jul 20, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
Myotonia congenita--a cause of muscle weakness and stiffness
Nicolas Chrestian1, Jack Puymirat, Jean-Pierre Bouchard
1University of Laval, QC, Canada.
Background:
A 56-year-old woman was referred to a neurogenetic clinic with a history of stiffness and transient weakness. A previous needle electromyogram had confirmed the presence of myotonia, but a muscle biopsy had revealed no evidence of dystrophy.
Investigations:
Neurological examination, electrophysiological studies and genetic testing.
Diagnosis:
Recessive myotonia congenita (Becker's disease).
Management:
Explanation of the nature of the disease and treatment with mexiletine 200 mg twice daily.
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