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:
- Síndrome de Walker Warburg
- Titinopatía dominante
- Miastenia Grave
- Parálisis Periódica Hipocalémica
- Miopatía nemalínica
- Ataxia de Friedreich
- Síndrome de MERRF
- GNE Myopathy
- Congenital Myopathy
- Primary Mitochondrial Myopathies
- Congenital Myasthenic Syndromes
- Andersen-Tawil Syndrome
- Centronuclear Myopathy
- Congenital Muscular Dystrophy
- Oculopharyngeal Muscular Dystrophy
- Distal Myopathy
- Collagen Type VI-Related Disorders
- X-Linked Myotubular Myopathy
- MELAS Syndrome
- 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
- 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
- Central Core Disease
- Werdnig-Hoffmann Disease
- 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
- Titinopatía recesiva
- Miopatía congénita por desproporción del tipo de fibra