Muscular Dystrophy Association
2024 Member
About Muscular Dystrophy Association
Muscular Dystrophy Association (MDA) is committed to transforming the lives of individuals living with muscular dystrophy, ALS and related neuromuscular diseases. Families are at the heart of MDA’s mission. A caring and concerned group of families started MDA in 1950, and we continue to relentlessly pursue our promise to transform the lives of people living with muscular dystrophy, ALS and related neuromuscular diseases, through research, care and advocacy. Read more about MDA’s journey and the progress we’ve helped make possible.
Related Rare Diseases:
- X-Linked Myopathy with Excessive Autophagy
- Walker Warburg Syndrome
- GNE Myopathy
- Congenital Myopathy
- Spinal Muscular Atrophy with Respiratory Distress Type 1
- Primary Mitochondrial Myopathies
- Congenital Myasthenic Syndromes
- Andersen-Tawil Syndrome
- Centronuclear Myopathy
- Congenital Muscular Dystrophy
- Oculopharyngeal Muscular Dystrophy
- Distal Myopathy
- Collagen Type VI-Related Disorders
- Spinal Muscular Atrophy
- Myofibrillar Myopathy
- Kennedy Disease
- X-Linked Myotubular Myopathy
- MERRF Syndrome
- MELAS Syndrome
- Fukuyama Type Congenital Muscular Dystrophy
- Carnitine Palmitoyltransferase 1A Deficiency
- Phosphoglycerate Kinase Deficiency
- Facioscapulohumeral Muscular Dystrophy
- Paramyotonia Congenita
- Mitochondrial Neurogastrointestinal Encephalopathy
- Limb-Girdle Muscular Dystrophies
- Lambert-Eaton Myasthenic Syndrome
- Hyperkalemia
- Hypokalemia
- Muscular Dystrophy Association
- Sporadic Inclusion Body Myositis
- Emery Dreifuss Muscular Dystrophy
- Kugelberg Welander Syndrome
- Pompe Disease
- Glycogen Storage Disease Type 7
- Glycogen Storage Disease Type V
- Myotonia Congenita
- Dejerine-Sottas Syndrome
- Myotonic Dystrophy
- Polymyositis and Necrotizing Myopathy
- Dermatomyositis
- Charcot-Marie-Tooth Disease
- Nemaline Myopathy
- Central Core Disease
- Amyotrophic Lateral Sclerosis
- Myasthenia Gravis
- Duchenne Muscular Dystrophy
- Werdnig-Hoffmann Disease
- Friedreich’s Ataxia
- Distrofia muscular de Duchenne
- Atrofia muscular espinal
- Enfermedad de Pompe
- Distrofia muscular congénita tipo Fukuyama
- Enfermedad de Kennedy
- Atrofia muscular espinal con dificultad respiratoria tipo 1
- Miopatía con autofagia excesiva ligada al cromosoma X
- Esclerosis lateral amiotrófica
- Miopatía miofibrilar
- Recessive Titinopathy
- Titinopatía recesiva
- Congenital Fiber Type Disproportion
- Miopatía congénita por desproporción del tipo de fibra
- Dominant Titinopathy
- Hypokalemic Periodic Paralysis
