myotonic dystrophy type 2

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Brain Structure and Clinical Endpoints in Myotonic Dystrophy Type 2	Cognition Disorders, Cognitive Dysfunction, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, cognitive disorder, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic dystrophy type 1, myotonic dystrophy type 2, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, psychiatric disorder	Enrolling by invitation	Not stated	2026-07-14		NCT05854433
Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Myotonic Dystrophy 2, facioscapulohumeral muscular dystrophy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic dystrophy type 1, myotonic dystrophy type 2, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease	Recruiting	Not stated	2025-10-15		NCT00082108

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