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Updated: Jan 19, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
Achalasia in a Patient with Myotonic Dystrophy
Hiroki Sato1, Ken-Ichi Mizuno1, Satoru Hashimoto1
1Division of Gastroenterology and Hepatology, Niigata University Medical and Dental Hospital, Japan.
Abstract:
Myotonic dystrophy is a progressive disorder mainly affecting the voluntary muscles. We herein report a rare case of myotonic dystrophy complicated with high-resolution manometry-defined achalasia, the pathology of which is absent relaxation of the smooth muscles of lower esophageal sphincter (LES). In the present case, achalasia was considered a complication of myotonic dystrophy instead of sporadic achalasia, as on performing high-resolution manometry, the finding of an impaired LES relaxation (myotonic phase) changed to a totally emaciated LES function (muscle weakness phase) as myotonic dystrophy progressed.
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