• Thumbnail for Muscular dystrophy
    Muscular dystrophies (MD) are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown...
    30 KB (2,269 words) - 03:51, 8 November 2024
  • Thumbnail for Duchenne muscular dystrophy
    Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy predominantly affecting boys. The onset of muscle weakness typically begins around...
    66 KB (6,597 words) - 08:13, 8 November 2024
  • Thumbnail for Facioscapulohumeral muscular dystrophy
    Facioscapulohumeral muscular dystrophy (FSHD) is a type of muscular dystrophy, a group of heritable diseases that cause degeneration of muscle and progressive...
    176 KB (16,456 words) - 00:30, 6 November 2024
  • Muscular Dystrophy Association (MDA) is an American nonprofit organization dedicated to supporting people living with muscular dystrophy, ALS, and related...
    47 KB (4,969 words) - 20:44, 23 November 2024
  • Thumbnail for Becker muscular dystrophy
    Becker muscular dystrophy (BMD) is an X-linked recessive inherited disorder characterized by slowly progressing muscle weakness of the legs and pelvis...
    26 KB (2,531 words) - 04:16, 2 November 2024
  • Thumbnail for Limb–girdle muscular dystrophy
    Limb–girdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of clinical characteristics....
    35 KB (2,822 words) - 01:57, 6 November 2024
  • Thumbnail for Oculopharyngeal muscular dystrophy
    Oculopharyngeal muscular dystrophy (OPMD) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old...
    20 KB (1,189 words) - 17:52, 7 September 2024
  • Muscular Dystrophy UK (MDUK) is a UK charity focusing on muscular dystrophy and related conditions. It works on behalf of those with over 60 muscle wasting...
    6 KB (560 words) - 17:10, 21 May 2024
  • Thumbnail for Fukuyama congenital muscular dystrophy
    Fukuyama congenital muscular dystrophy (FCMD) is a rare, autosomal recessive form of muscular dystrophy (weakness and breakdown of muscular tissue) mainly...
    12 KB (1,218 words) - 14:54, 21 August 2024
  • include: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) Myotonic dystrophy Limb-Girdle (LGMD) Facioscapulohumeral dystrophy (FSHD) Congenital...
    15 KB (1,733 words) - 23:05, 12 November 2024
  • Thumbnail for Emery–Dreifuss muscular dystrophy
    Emery–Dreifuss muscular dystrophy (EDMD) is a type of muscular dystrophy, a group of heritable diseases that cause progressive impairment of muscles....
    21 KB (1,627 words) - 01:14, 24 October 2024
  • Thumbnail for Congenital muscular dystrophy
    Congenital muscular dystrophies are autosomal recessively-inherited muscle diseases. They are a group of heterogeneous disorders characterized by muscle...
    34 KB (3,524 words) - 14:14, 13 August 2024
  • disorders. Duchenne muscular dystrophy Becker muscular dystrophy DMD-associated dilated cardiomyopathy Limb girdle muscular dystrophies (LGMD) as defined...
    9 KB (902 words) - 15:36, 8 September 2024
  • Thumbnail for Myotonic dystrophy
    Myotonic dystrophy (DM) is a type of muscular dystrophy, a group of genetic disorders that cause progressive muscle loss and weakness. In DM, muscles are...
    43 KB (4,557 words) - 07:24, 11 November 2024
  • Thumbnail for Trapezius
    muscle is one of the commonly affected muscles in facioscapulohumeral muscular dystrophy (FSHD). The lower and middle fibers are affected initially, and the...
    13 KB (1,352 words) - 17:48, 19 August 2024
  • Thumbnail for Ullrich congenital muscular dystrophy
    Ullrich congenital muscular dystrophy (UCMD) is a form of congenital muscular dystrophy. There are two forms: UCMD1 and UCMD2. UCMD1 is associated with...
    15 KB (1,320 words) - 14:36, 24 August 2024
  • phenotype similar to the less severe Becker muscular dystrophy (BMD). In the case of Duchenne muscular dystrophy, the protein that becomes compromised is...
    10 KB (1,192 words) - 22:57, 11 November 2024
  • Thumbnail for Arthrogryposis
    the different types of AMC include: Arthrogryposis multiplex due to muscular dystrophy. Arthrogryposis ectodermal dysplasia other anomalies, also known as...
    35 KB (3,588 words) - 19:20, 22 July 2024
  • in the United States to raise money for the Muscular Dystrophy Association (MDA). The Muscular Dystrophy Association was founded in 1950 with hopes of...
    114 KB (12,651 words) - 11:20, 17 November 2024
  • locations. Service Merchandise was a large corporate donor to the Muscular Dystrophy Association. Chairman/CEO Raymond Zimmerman would appear multiple...
    13 KB (1,225 words) - 21:42, 22 November 2024
  • Thumbnail for Dystrophin
    Dystrophin (category Muscular dystrophy)
    dystrophin gene can cause different forms of muscular dystrophy, a disease characterized by progressive muscular wasting. The most common of these disorders...
    21 KB (2,466 words) - 09:28, 3 July 2024
  • heredity. Muscular dystrophy Duchenne muscular dystrophy Becker's muscular dystrophy Myotonic dystrophy Reflex neurovascular dystrophy Retinal dystrophy Cone...
    776 bytes (96 words) - 04:14, 1 September 2024
  • Thumbnail for Nutritional muscular dystrophy
    Nutritional Muscular Dystrophy (Nutritional Myopathy or White Muscle Disease) is a disease caused by a deficiency of selenium and vitamin E in dietary...
    8 KB (928 words) - 12:53, 11 June 2024
  • results with a new gene therapy candidate for patients with Limb-Girdle muscular dystrophy; two months after receiving a single treatment, muscles from all three...
    18 KB (1,732 words) - 21:45, 28 October 2024
  • Gowers's sign (category Muscular dystrophy)
    Duchenne muscular dystrophy where it is mostly evident at 4–6 years, but also presents itself in centronuclear myopathy, myotonic dystrophy and various...
    2 KB (164 words) - 12:16, 4 September 2024
  • Thumbnail for LAMA2 related congenital muscular dystrophy
    LAMA2 muscular dystrophy (LAMA2-MD) is a genetically determined muscle disease caused by pathogenic mutations in the LAMA2 gene. It is a subtype of a larger...
    36 KB (3,710 words) - 08:53, 9 November 2024
  • been approved to treat specific groups of mutations causing Duchenne muscular dystrophy. In September 2016, eteplirsen (ExonDys51) received FDA approval for...
    25 KB (2,476 words) - 03:39, 19 November 2024
  • Types of Distal MD". Muscular Dystrophy Association. 2015-12-18. Retrieved 2019-04-16. "OMIM Entry - # 310200 - MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD"...
    43 KB (995 words) - 08:29, 11 November 2024
  • Thumbnail for Spinal muscular atrophy
    who first documented the late-onset form and distinguished it from muscular dystrophy. Very rarely used Dubowitz disease (not to be confused with Dubowitz...
    90 KB (10,015 words) - 03:08, 25 November 2024
  • Thumbnail for Jerry Lewis
    Hour to host of The Jerry Lewis Labor Day Telethon (benefiting the Muscular Dystrophy Association), Lewis performed in concert stages, nightclubs, audio...
    181 KB (17,558 words) - 02:37, 22 November 2024