MYOTONIC DYSTROPHY, CONGENITAL
Clinical trials for MYOTONIC DYSTROPHY, CONGENITAL explained in plain language.
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Can music and movement ease symptoms of a rare muscle disease in kids?
Symptom relief Recruiting nowThis study is testing whether weekly music and movement sessions are practical and helpful for children with congenital myotonic dystrophy type 1 (DM1), a rare genetic disorder that affects muscles, the brain, and the heart. Researchers will see if these sessions can improve phys…
Matched conditions: MYOTONIC DYSTROPHY, CONGENITAL
Phase: NA • Sponsor: Hanns Lochmuller • Aim: Symptom relief
Last updated Mar 31, 2026 12:11 UTC
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Spain launches major effort to map a rare muscle disease
Knowledge-focused Recruiting nowThis study is creating a national patient registry in Spain for people with Myotonic Dystrophy Type 1 (DM1), a rare genetic muscle disease. It aims to collect detailed health information from up to 3,000 participants to better understand how the disease varies and progresses over…
Matched conditions: MYOTONIC DYSTROPHY, CONGENITAL
Sponsor: Fundació Institut Germans Trias i Pujol • Aim: Knowledge-focused
Last updated Mar 27, 2026 12:40 UTC