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Becker muscular dystrophy
Other Names for this Disease
- Becker's muscular dystrophy
- Benign pseudohypertrophic muscular dystrophy
- Muscular dystrophy pseudohypertrophic progressive, Becker type
- Muscular dystrophy, Becker type
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 The age of onset and rate of progression can vary among affected people. Muscle weakness usually becomes apparent between the ages of 5 and 15. In some cases, heart involvement (cardiomyopathy) is the first sign. BMD is caused by a mutation in the DMD gene and is inherited in an X-linked recessive manner. BMD is very similar to Duchenne muscular dystrophy, except that symptoms begin later and progress at a slower rate. There is no cure for this condition, and treatment aims to relieve symptoms to help quality of life. People with BMD may survive into their 40s or beyond.Becker muscular dystrophy (BMD) is an inherited condition that primarily affects males and causes progressive weakness and wasting of the skeletal and cardiac (heart) muscles.
Last updated: 3/5/2014
- Duchenne and Becker muscular dystrophy. Genetics Home Reference. February, 2012; http://www.ghr.nlm.nih.gov/condition/duchenne-and-becker-muscular-dystrophy. Accessed 3/5/2014.
- C Boulay, Brigitte Chabrol. Duchenne and Becker muscular dystrophy. Orphanet. August, 2007; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=262. Accessed 3/5/2014.
- Kaneshiro NK, Hoch DB. Becker's muscular dystrophy. MedlinePlus. 2008; http://www.nlm.nih.gov/medlineplus/ency/article/000706.htm. Accessed 11/18/2009.
- Genetics Home Reference (GHR) contains information on Becker muscular dystrophy. This website is maintained by the National Library of Medicine.
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- The Merck Manuals Online Medical Library provides information on this condition. Click on the link to view the information.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
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- The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Becker muscular dystrophy. Click on the link to view a sample search on this topic.