Medical condition factsheets from the Muscular Dystrophy Campaign are listed below.

See also: medical issues factsheets and living issues factsheets

Becker muscular dystrophy

This factsheet outlines the features associated with Becker muscular dystrophy, including diagnostic information, disease progression, and inheritance issues

Charcot-Marie-Tooth disease

Factsheet outlining Charcot-Marie-Tooth disease, the different types, causes and how it is passed on. Charcot-Marie-Tooth disease does not describe a single disorder, but a group of conditions that are superficially similar.

Central core disease factsheet

This factsheet contains information about central core disease

Congenital fibre type disproportion

Congenital fibre type disproportion myopathy factsheet

Minicore (multicore) myopathy

The factsheet describes congenital myopathies especially minicore (multicore), how it presents, progresses, inheritance patterns and treatment.

Myotubular (centronuclear) myopathy

This factsheet describes myopathies especially myotubular (centronuclear), how it presents, inheritance patterns, how the condition is diagnosed, rate of progression and treatment.

Nemaline myopathy

The factsheet describes congenital myopathies - especially nemaline. It covers how nemaline presents, inheritance patterns, recent genetic advances, how it is diagnosed, its progression and treatment.

Congenital myotonic dystrophy

Factsheet describes myotonic dystrophy, its rarity, symptoms, diagnosis, inheritance patternsand treatment.

Duchenne muscular dystrophy

Factsheet outlining the features associated with Duchenne muscular dystrophy, including diagnostic information, disease progression, and inheritance issues

Duchenne muscular dystrophy: the older child

Factsheet outlines some of the issues surrounding boys over eight with Duchenne and how the condition may affect their mobility. It focuses on their needs in school, home, post school education / employment, medical surveillance and respite care.

Emery-Dreifuss muscular dystrophy

Factsheet outlining Emery-Dreifuss muscular dystrophy, how and which muscles it affects, how the condition can be improved, inheritance and similar conditions.

Facioscapulohumeral muscular dystrophy

Factsheet outlining FSH muscular dystrophy, diagnosis, inheritance and other issues surrounding the condition

Inclusion body myositis

A factsheet that describes what inclusion body myositis is, how the condition is caused and how a diagnosis is made

Juvenile dermatomyositis

A factsheet that describes what dermatomyositis is, its symptoms, diagnosis, and treatment

Manifesting carriers of Duchenne muscular dystrophy

This factsheet explains about the manifestering carriers of duchenne md, their symptoms, diagnosis and other problems surrounding the condition.

McArdle’s disease

Factsheet describes McArdle's disease, symptoms, exercise and treatment and other issues surrounding the condition.

Mitochondrial myopathies

Factsheet describing mitochondral myopathies, causes, diagnosis, treatment and other issues surrounding the condition.

Myasthenia Gravis

A factsheet that describes Myasthenia Gravis, chances of developing the condition, symptoms and causes, classification of Myasthenia Gravis, treatment and other issues surrounding the condition.

Myopathy

Factsheet describes myopathy, causes, diagnosis and problems associated with the condition.

Fibrodysplasia Ossificans Progressiva (FOP)

A factsheet on Fibrodysplasia Ossificans Progressiva (FOP), progression, muscles affected, inheritance patterns and treatment.

Myotonic dystrophy

Factsheet describing myotonic dystrophy, its inheritance patterns, causes, future advances, problems and management of the condition.

Oculopharyngeal muscular dystrophy (OPMD)

Factsheet describing oculopharyngeal muscular dystrophy (OPMD), sympyoms and signs, inheritance patterns, diagnosis and management.

Periodic paralyses

Factsheet describes periodic paralyses, symptoms, the different types, causes, inheritance patterns and treatment.

Polymyositis, dermatomyositis and sarcoid myopathy

Factsheet describing polymyositis, dermatomyositis and sarcoid myopathy, symptoms, diagnosis and treatment.

Limb girdle muscular dystrophy

Factsheet outlining the features associated with limb girdle muscular dystrophy, how it is diagnosed and the different types of both recessive and dominant limb girdle muscular dystrophy

Myotonias

Factsheet describes myotonia, its inheritance patterns, causes and other forms of myotonia.

Congenital muscular dystrophies

A factsheet, written by the team at Hammersmith Hospital, about congenital muscular dystrophy

Congenital muscular dystrophy with rigidity of the spine, including RSMD1

Information about congenital muscular dystrophy with rigidity of the spine, including RSMD1

Merosin-deficient congenital muscular dystrophy(MDC1A)

Information about merosin-deficient congenital muscular dystrophy

Ullrich congential muscular dystrophy

Information about Ullrich congenital muscular dystrophy, how it is diagnosed and how it affects people who have it

Metabolic disorders that cause pain and/or weakness on exercise

A factsheet by Professor D.M Turnbull on metabolic disorders that cause pain and/or weakness on exercise.

Bethlem myopathy factsheet

Factsheet on Bethlem myopathy