Neuromuscular conditions covered by the Muscular Dystrophy Campaign
On this page are listed all of the neuromuscular conditions covered by the charity. There is a dedicated homepage for each of the more common conditions (see list on About your condition page). To find out about spinal muscular atrophy please visit The Jennifer Trust website at: www.jtsma.org.uk
Where details are known, links to support group websites are listed here. See also our links pages.
If you know of other support groups, please email web@muscular-dystrophy.org
Muscular dystrophies
- Congenital muscular dystrophies
- Duchenne muscular dystrophy (DMD)
- Becker muscular dystrophy (BMD)
- Emery-Dreifuss syndrome (scapuloperoneal md)
- Facioscapulohumeral muscular dystrophy (FSH)
- Oculopharyngeal muscular dystrophy
- Limb-girdle muscular dystrophies
Support groups: Duchenne Family Support Group, Parent Project UK Duchenne muscular dystrophy, FSH Support Group, Oculopharyngeal muscular dystrophy (OPDM) Support Group
Myotonic disorders
- Myotonic dystrophy type 1 and 2
- Congenital myotonic dystrophy
- Myotonia congenita dominant type - Thomsen, recessive type - Becker)
- Parayotonia congenita
- Schwartz-Jampel syndrome
- Pseudomyotonia
- Neuromyotonia (continuous muscle fibre activity - Isaacs)
Support group: Myotonic Dystrophy Support Group
Congenital myopathy
- Central core disease
- Multimini core disease
- Nemaline myopathy
- Myotubular (centronuclear) myopathy
- Fibre-type disproportion
- Non-specific myopathy
Mitochondrial myopathies
- Defects of mitochondrial substrate utilisation
- Defects of the respiratory chain
- Defects of energy conservation and transduction
Email the support group: Mitochondrial Myopathies Support Group
Lipid storage myopathies
- Carnitine deficiency
- Carnitine palmityl transferase deficiency
- Myoadenylate deaminase deficiency
Inherited metabolic myopathies
- Glycogen storage disease of muscle
- Type II (Pompe's disease - acid maltase deficiency)
- Type III (Cori Forbes - debrancher enzyme deficiency)
- Type IV (Andersen - brancher enzyme deficiency)
- Type V (McArdle - phosphorylase deficiency)
- Type VII (Tarui - phosphofructokinase deficiency)
Support groups: CLIMB (Children Living with Inherited Metabolic Diseases) and Association for Glycogen Storage Disease
Periodic paralysis (muscle channelopathies
Myositis
- Dermatomyositis
- Juvenile dermatomyositis
- Polymyositis
- Polymyositis in association with collagen or connective tissue disease
- Inclusion body myositis
Support group: Myositis Support Group
Spinal muscular atrophies (SMA)
- Severe SMA (Werdnig Hoffman disease - type I)
- Intermediate SMA (Type II)
- Mild SMA (Kugelberg Welander disease - type III)
- Adult SMA
- X-linked bulbospinal neuropathy (Kennedy's syndrome
- Dominant SMA variants
Support Group: The Jennifer Trust for SMA
Hereditary neuropathies
- Charcot-Marie-Tooth disease
- Peroneal muscular atrophy
Support group: Charcot-Marie-Tooth United Kingdom
Inflammatory & auto-immune neuropathies
- Acute post infective polyneuropathy (Guillan Barre syndrome)
- Chronic inflammatory demyelinating peripheral neuropathy (CIDP)
- Serum neuropathy
Support group: Guillain-Barré syndrome support group
Disorders of the neuromuscular junction
- Myasthenia Gravis
- Congenital myasthenic syndromes
Support Group: The Myasthenia Gravis Association

