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Select A Muscle Disease

A

Acid Maltase Deficiency (AMD)
Amyotrophic Lateral Sclerosis (ALS)
Andersen-Tawil Syndrome

B

Becker Muscular Dystrophy (BMD)
Becker Myotonia Congenita
Bethlem Myopathy
Bulbospinal Muscular Atrophy (Spinal-Bulbar Muscular Atrophy)

C

Carnitine Deficiency
Carnitine Palmityl Transferase Deficiency (CPT Deficiency)
Central Core Disease (CCD)
Centronuclear Myopathy
Charcot-Marie-Tooth Disease (CMT)
Congenital Muscular Dystrophy (CMD)
Congenital Myasthenic Syndromes (CMS)
Congenital Myotonic Dystrophy
Cori Disease (Debrancher Enzyme Deficiency)

D

Debrancher Enzyme Deficiency
Dejerine-Sottas Disease (DSD)
Dermatomyositis (DM)
Distal Muscular Dystrophy (DD)
Duchenne Muscular Dystrophy (DMD)
Dystrophia Myotonica (Myotonic Muscular Dystrophy)

E

Emery-Dreifuss Muscular Dystrophy (EDMD)
Endocrine Myopathies
Eulenberg Disease (Paramyotonia Congenita)

F

Facioscapulohumeral Muscular Dystrophy (FSH or FSHD)
Finnish (Tibial) Distal Myopathy
Forbes Disease (Debrancher Enzyme Deficiency)
Friedreich’s Ataxia (FA)
Fukuyama Congenital Muscular Dystrophy

G

Glycogenosis Type 10
Glycogenosis Type 11
Glycogenosis Type 2
Glycogenosis Type 3
Glycogenosis Type 5
Glycogenosis Type 7
Glycogenosis Type 9
Gowers-Laing Distal Myopathy

H

Hauptmann-Thanheuser MD (Emery-Dreifuss Muscular Dystrophy)
Hereditary Inclusion-Body Myositis
Hereditary Motor and Sensory Neuropathy (Charcot-Marie-Tooth Disease)
Hyperthyroid Myopathy
Hypothyroid Myopathy

I

Inclusion-Body Myositis (IBM)
Inherited Myopathies
Integrin-Deficient Congenital Muscular Dystrophy

K

Kennedy Disease (Spinal-Bulbar Muscular Atrophy)
Kugelberg-Welander Disease (Spinal Muscular Atrophy)

L

Lactate Dehydrogenase Deficiency
Lambert-Eaton Myasthenic Syndrome (LEMS)
Limb-Girdle Muscular Dystrophy (LGMD)
Lou Gehrig’s Disease (Amyotrophic Lateral Sclerosis)

M

McArdle Disease (Phosphorylase Deficiency)
Merosin-Deficient Congenital Muscular Dystrophy
Metabolic Diseases of Muscle
Mitochondrial Myopathy
Miyoshi Distal Myopathy
Motor Neurone Disease
Muscle-Eye-Brain Disease
Myasthenia Gravis (MG)
Myoadenylate Deaminase Deficiency
Myofibrillar Myopathy
Myophosphorylase Deficiency
Myotonia Congenita (MC)
Myotonic Muscular Dystrophy (MMD)
Myotubular Myopathy (MTM or MM)

N

Nemaline Myopathy
Nonaka Distal Myopathy

O

Oculopharyngeal Muscular Dystrophy (OPMD)

P

Paramyotonia Congenita
Pearson Syndrome
Periodic Paralysis
Peroneal Muscular Atrophy (Charcot-Marie-Tooth Disease)
Phosphofructokinase Deficiency
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Phosphorylase Deficiency
Polymyositis (PM)
Pompe Disease (Acid Maltase Deficiency)
Progressive External Ophthalmoplegia (PEO)

R

Rod Body Disease (Nemaline Myopathy)

S

Spinal Muscular Atrophy (SMA)
Spinal-Bulbar Muscular Atrophy (SBMA)
Steinert Disease (Myotonic Muscular Dystrophy)

T

Tarui Disease (Phosphofructokinase Deficiency)
Thomsen Disease (Myotonia Congenita)

U

Ullrich Congenital Muscular Dystrophy

W

Walker-Warburg Syndrome (Congenital Muscular Dystrophy)
Welander Distal Myopathy
Werdnig-Hoffmann Disease (Spinal Muscular Atrophy)

Z

ZASP-Related Myopathy

MDA in Your Community

Publications

In Focus: Spinal Muscular Atrophy (PDF)
Standard of Care in Spinal Muscular Atrophy
Spinal Muscular Atrophy Care Guidelines
Facts About Spinal Muscular Atrophy
Facts About Genetics and Neuromuscular Diseases
Learning to Live with Neuromuscular Disease: A Message for Parents
A Teacher's Guide to Neuromuscular Disease
Great Expectations: Pregnancy Series (PDF)

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Muscular Dystrophy Association — USA
National Headquarters
3300 E. Sunrise Drive
Tucson, AZ 85718
(800) 572-1717

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