Emery-Dreifuss muscular dystrophy 2, autosomal dominant | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History Study for Charcot Marie Tooth Disease	Charcot-Marie-Tooth Disease, Type IA, Charcot-Marie-Tooth Disease, Type IB, Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease axonal type 2H, Charcot-Marie-Tooth disease axonal type 2N, Charcot-Marie-Tooth disease type 1C, Charcot-Marie-Tooth disease type 1D, Charcot-Marie-Tooth disease type 1E, Charcot-Marie-Tooth disease type 1F, Charcot-Marie-Tooth disease type 2, Charcot-Marie-Tooth disease type 2A1, Charcot-Marie-Tooth disease type 2A2, Charcot-Marie-Tooth disease type 2B1, Charcot-Marie-Tooth disease type 2B2, Charcot-Marie-Tooth disease type 2B5, Charcot-Marie-Tooth disease type 2D, Charcot-Marie-Tooth disease type 2E, Charcot-Marie-Tooth disease type 2I, Charcot-Marie-Tooth disease type 2J, Charcot-Marie-Tooth disease type 2R, Charcot-Marie-Tooth disease type 2T, Charcot-Marie-Tooth disease type 2Y, Charcot-Marie-Tooth disease type 4A, Charcot-Marie-Tooth disease type 4B1, Charcot-Marie-Tooth disease type 4B2, Charcot-Marie-Tooth disease type 4B3, Charcot-Marie-Tooth disease type 4C, Charcot-Marie-Tooth disease type 4D, Charcot-Marie-Tooth disease type 4E, Charcot-Marie-Tooth disease type 4H, Charcot-Marie-Tooth disease, Type 2A, Charcot-Marie-Tooth disease, Type 2K, Charcot-Marie-Tooth disease, Type 4A, axonal form, Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Emery-Dreifuss muscular dystrophy 2, autosomal dominant, Hereditary Motor and Sensory Neuropathy, Type IIC, Pathologic Processes, Pathological Conditions, Signs and Symptoms, autosomal dominant Charcot-Marie-Tooth disease type 2K, central nervous system malformation, disease, hereditary disease, hereditary motor and sensory neuropathy, hereditary neuropathy with liability to pressure palsies, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy	Recruiting	Not stated	2026-09-17		NCT05902351
Long-Term Development of Muscular Dystrophy Outcome Assessments	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Emery-Dreifuss muscular dystrophy 2, autosomal dominant, Eye Diseases, Hereditary, Limb-girdle muscular dystrophy, type 2E, Malformations of Cortical Development, Group II, Muscular Disorders, Atrophic, Muscular Dystrophy, Limb-Girdle, Type 1C, Muscular Dystrophy, Limb-Girdle, Type 1E, Respiration Disorders, autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6), autosomal dominant limb-girdle muscular dystrophy type 1F, autosomal dominant limb-girdle muscular dystrophy type 1G, autosomal dominant limb-girdle muscular dystrophy type 1H, autosomal recessive limb-girdle muscular dystrophy type 2A, autosomal recessive limb-girdle muscular dystrophy type 2B, autosomal recessive limb-girdle muscular dystrophy type 2C, autosomal recessive limb-girdle muscular dystrophy type 2F, autosomal recessive limb-girdle muscular dystrophy type 2G, autosomal recessive limb-girdle muscular dystrophy type 2I, autosomal recessive limb-girdle muscular dystrophy type 2J, autosomal recessive limb-girdle muscular dystrophy type 2L, autosomal recessive limb-girdle muscular dystrophy type 2M, autosomal recessive limb-girdle muscular dystrophy type 2N, autosomal recessive limb-girdle muscular dystrophy type 2O, autosomal recessive limb-girdle muscular dystrophy type 2P, autosomal recessive limb-girdle muscular dystrophy type 2Q, autosomal recessive limb-girdle muscular dystrophy type 2T, autosomal recessive limb-girdle muscular dystrophy type 2U, autosomal recessive limb-girdle muscular dystrophy type 2W, autosomal recessive limb-girdle muscular dystrophy type 2X, autosomal recessive limb-girdle muscular dystrophy type 2Y, autosomal recessive limb-girdle muscular dystrophy type R18, cardiomyopathy, cardiovascular disorder, central nervous system malformation, cerebral cortical dysplasia, cobblestone lissencephaly, eye disorder, heart disorder, hereditary disease, inherited neurodegenerative disorder, limb-girdle muscular dystrophy, lissencephaly spectrum disorders, muscle tissue disorder, muscular dystrophy, muscular dystrophy-dystroglycanopathy, type A, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, respiratory system disorder, sarcoglycanopathy	Recruiting	Not stated	2025-11-18		NCT05989620