ICD G71.11ORPHA:273DM1

Myotonic Dystrophy

Myotonic dystrophy type 1 is the most common adult-onset muscular dystrophy, causing progressive muscle weakness, myotonia (difficulty relaxing muscles), and multi-system complications including heart rhythm problems and cataracts. It is caused by a DMPK gene expansion. There is currently no cure, but management can significantly improve quality of life.

550
Articles
155
Trials (11 AU)
Updated
26 March 2026
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Common Questions

What is Myotonic Dystrophy?

Myotonic dystrophy type 1 is the most common adult-onset muscular dystrophy, causing progressive muscle weakness, myotonia (difficulty relaxing muscles), and multi-system complications including heart rhythm problems and cataracts. It is caused by a DMPK gene expansion. There is currently no cure, but management can significantly improve quality of life.

How many clinical trials are available for Myotonic Dystrophy?

RareWays currently indexes 155 clinical trials for Myotonic Dystrophy, of which 43 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Myotonic Dystrophy come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

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