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Langer-Giedion Syndrome
The goal of this page is to consolidate information and resources on Langer Giedion Syndrome. It will be updated as often as possible. I hope it will be a site that research scientists, clinicians, M.D.'s as well as affected individuals and their families will find useful.
http://wimp.nsm.uh.edu/lgs.html
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Langer-Giedion Syndrome Association
http://www.geocities.com/HotSprings/9308/
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NORD - Trichorhinophalangeal Syndrome Type II
Trichorhinophalangeal Syndrome Type II (TRPS2), also known as Langer-Giedion Syndrome, is an extremely rare inherited multisystem disorder. TRPS2 is characterized by fine, thin hair; unusual facial features; progressive growth retardation resulting in short stature (dwarfism); abnormally short fingers and toes (brachydactyly); "cone-shaped" formation of the "growing ends" of certain bones (epiphyseal coning); and/or development of multiple bony growths (exostoses) projecting outward from the surfaces of various bones of the body.
http://www.stepstn.com/cgi-win/nord.exe?proc=Redirect&type=rdb_sum&id=1074.htm#synonyms
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NORD - Trichorhinophalangeal Syndrome Type II
The information contained in the Rare Disease Database (RDB) is provided for educational purposes only. It should not be used for diagnostic or treatment purposes. If you order the full text version of this report from NORD, you can contact the agencies listed in the Resources section for more detailed information and avenues to support. In addition, your personal physician may be able to provide details specific to your case.
http://www.stepstn.com/nord/rdb_sum/1074.htm
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