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Leri Weill dyschondrosteosis
Other Names for this Disease
- Léri-Weill dyschondrosteosis
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skeletal dysplasia characterized by short stature and an abnormality of the wrist bones called Madelung deformity. Short stature is present from birth due to shortening of the bones in the forearms and lower legs. Madelung deformity typically develops during mid-to-late childhood and may progress during puberty. People with this condition often experience pain in their wrists or arms. The severity of Leri Weill dyschondrosteosis varies among affected individuals, although the signs and symptoms of this condition are generally more severe in females. Other features of Leri Weill dyschondrosteosis can include increased muscle size, elbow abnormalities, scoliosis, high-arched palate, and exostoses. Intelligence is not affected by this condition. In around 70 percent of cases, Leri Weill dyschondrosteosis is caused by mutations in or near one copy of the SHOX gene in each cell. The cause of the disorder remains unknown in the remaining 30 percent of cases.Leri Weill dyschondrosteosis is a
Last updated: 2/23/2010
- Heath K. Léri-Weill dyschondrosteosis. Orphanet Web site. May 2009; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=240. Accessed 2/23/2010.
- Munns C, Glass I. SHOX-Related Haploinsufficiency Disorders. GeneReviews Web site. February 1, 2008; http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd. Accessed 2/23/2010.
- SHOX. Genetics Home Reference Web site. May 2008; http://ghr.nlm.nih.gov/gene=shox. Accessed 2/23/2010.
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- Genetics Home Reference (GHR) contains information on Leri Weill dyschondrosteosis. This website is maintained by the National Library of Medicine.
- 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) database contains genetics resources that discuss Leri Weill dyschondrosteosis. Click on the link to go to OMIM and review these resources.
- 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 Leri Weill dyschondrosteosis. Click on the link to view a sample search on this topic.