Leri Weill dyschondrosteosis
Other Names for this Disease
- Léri-Weill dyschondrosteosis
- Léri-Weill syndrome
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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.
- Genetics Home Reference (GHR) contains information on Leri Weill dyschondrosteosis. This website is maintained by the National Library of Medicine.
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- Online Mendelian Inheritance in Man (OMIM) is a 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.
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