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There is a page named "Becker muscular dystrophy" on Wikipedia
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
muscular dystrophies include Becker muscular dystrophy, facioscapulohumeral muscular dystrophy, and myotonic dystrophy, whereas limb–girdle muscular dystrophy...30 KB (2,269 words) - 03:51, 8 November 2024
Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy predominantly affecting boys. The onset of muscle weakness typically begins around...68 KB (6,768 words) - 07:29, 15 January 2025- Muscular Dystrophy Association (MDA) is an American nonprofit organization dedicated to supporting people living with muscular dystrophy, ALS, and related...47 KB (4,963 words) - 02:21, 22 December 2024
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- include: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) Myotonic dystrophy Limb-Girdle (LGMD) Facioscapulohumeral dystrophy (FSHD) Congenital...15 KB (1,733 words) - 04:11, 11 December 2024
- Gowers's sign (category Muscular dystrophy)conditions associated with proximal muscle weakness, including Becker muscular dystrophy, dermatomyositis and Pompe disease. For this maneuver, the patient...2 KB (164 words) - 12:16, 4 September 2024
- phenotype similar to the less severe Becker muscular dystrophy (BMD). In the case of Duchenne muscular dystrophy, the protein that becomes compromised...10 KB (1,192 words) - 22:57, 11 November 2024
Dystrophin (category Muscular dystrophy)referred to as muscular dystrophy. The deletions of one or several exons of the dystrophin DMD gene cause Duchenne and Becker muscular dystrophies. The large...21 KB (2,466 words) - 09:28, 3 July 2024- is remembered for his studies of muscular dystrophies. Becker's muscular dystrophy (OMIM 300376) and Becker myotonia (OMIM 255700) are named after him...3 KB (314 words) - 18:03, 10 February 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
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- 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
- Dystrophinopathy (category Muscular dystrophy)The severe end of the spectrum includes Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and DMD-associated dilated cardiomyopathy...3 KB (169 words) - 12:44, 6 August 2024
Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013provide for research with respect to various forms of muscular dystrophy, including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic...13 KB (1,183 words) - 00:40, 10 May 2023
Glycogen storage disease (redirect from Muscular phosphorylase kinase deficiency)glycogenosis related to dystrophy gene deletion: patient has a previously undescribed myopathy associated with both Becker muscular dystrophy and a glycogen storage...69 KB (6,188 words) - 20:52, 10 January 2025
Muscle hypertrophy (redirect from Muscular hypertrophy)infiltration of fat or other tissue). For instance, Duchenne and Becker muscular dystrophy may start as true muscle hypertrophy, but later develop into pseudohypertrophy...32 KB (3,542 words) - 20:57, 13 November 2024- provide for research with respect to various forms of muscular dystrophy, including Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic...4 KB (476 words) - 18:28, 23 November 2023
- Myotonia congenita (redirect from Batten Turner muscular dystrophy)Paramyotonia congenita Hyperkalemic periodic paralysis Dystrophies Myotonic dystrophy (myotonic muscular dystrophy: Type 1 and Type 2) Potassium channel disorders...26 KB (3,125 words) - 11:58, 6 October 2024
and Genetics. While in Children, Neuromuscular diseases such as Becker muscular dystrophy, including X-linked genetic disorder, are directly linked with...26 KB (2,418 words) - 23:56, 27 November 2024
- Becker's muscular dystrophy Named after Peter Emil Becker, German doctor who published an article about it in 1955. Becker muscular dystrophy (uncountable)
- Muscular dystrophy Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy Benign [Becker] muscular dystrophy
- cells include diabetes, traumatic spinal cord injury, Duchenne's muscular dystrophy, heart disease, and vision and hearing loss. Stem cells have the remarkable
- patients with Becker muscular dystrophy” by Sven et al. (2008) as part of an assignment for the University of Canberra. Becker muscular dystrophy (BMD) is