Geneticalliance.org langergiedion syndrome Also known as Trichorhinophalangeal syndrome, Type IISupport Groups langer-giedion syndrome Association 89 Ingham Avenue http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t
Geneticalliance.org langergiedion syndrome Association Conditions Served langer-giedion syndrome.Late Onset Tay-Sachs Foundation Conditions Served Tay-Sachs, Late Onset http://www.geneticalliance.org/ws_display.asp?filter=diseases_support_groups&key
Extractions: Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses. Mental retardation and abnormalities of chromosome 8 are often present. The exostoses in this syndrome appear identical to those of hereditary multiple exostoses (EXOSTOSES, HEREDITARY MULTIPLE). Synonyms and Source Vocabularies:
Extractions: Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Fennell, S. J. Articles by Czepulkowski, B. Journal of Medical Genetics, 1989, Vol 26, 167-171 SJ Fennell, JW Benson, AD Kindley, MJ Schwarz and B Czepulkowski
Extractions: Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Le Merrer, M. Articles by Maroteaux, P. Journal of Medical Genetics, 1992, Vol 29, 713-715 M Le Merrer, K Ben Othmane, V Stanescu, S Lyonnet, L Van Maldergem, G Royer, A Munnich and P Maroteaux Unite de Recherches sur les Handicaps Genetiques de l'Enfant, U12 INSERM, Hopital des Enfants Malades, Paris, France. Hereditary multiple exostoses is a dominantly inherited skeletal disorder which alters enchondral bone during growth and is characterised by exostoses of the juxta-epiphyseal regions. Using polymorphic DNA probes, we
LGCR (syn. Of Langer-Giedion Syndrome) ThirdAid.com the world s first dedicated online patient to patient medical helpcommunity. http://www.thirdaid.com/conditions/LGCR.htm
Musculoskeletal Diseases langergiedion syndrome. langer-giedion syndrome Association Langer-GiedionSyndrome Information - OMIM. Disease genes on Chromosome 8 - GeneCards http://www.mic.ki.se/Diseases/C05.html
Extractions: Diseases and Disorders Links pertaining to Musculoskeletal Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Achondroplasia Achondroplasia Acquired Hyperostosis Syndrome Acrocephalosyndactylia ... Tietze's Syndrome Musculoskeletal Diseases Textbook of Orthopaedics [CR Wheeless] Educational textbook syllabus [Borrill et al.] - Orthoteers (UK) The Belgian OrthoWeb - (BE) Site Map of the Orthopaedics and Sports Medicine resource at Univ of Washington, Seattle (US) The American Academy of Orthopaedic Surgeons A Musculoskeletal Atlas , an illustrated Musculoskeletal Glossary , and a set of educational cases (radiol.) - U of Washington (US) Ortho Supersite OrthoLinx WorldOrtho including A Simple Guide to Orthopaedics [RL Huckstep] - Nepean Hosp., Sydney (AU) A collection of Case discussions at OrthoGate.org
Extractions: This Article P Rs: Submit a response Alert me when this article is cited Alert me when P ... Alert me if a correction is posted Services E-mail this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Wilson, W. G. Articles by Aylsworth, A. S. WG Wilson, RT Herrington and AS Aylsworth A 22-year-old woman with the Langer-Giedion syndrome and delayed puberty is presented. Pertinent features include a bulbous nose, sparse hair, protruding ears, multiple cartilaginous exostoses, cone-shaped phalangeal epiphyses, short stature, microcephaly, and mental retardation. She is the oldest patient thus far described with this condition, and is compared to the ten previously published cases. The clinical course of patients with the Langer-Giedion syndrome and the possibility of malignant change in the exostoses have not been established.
Orthoguide.com Langer-Giedion Syndrome Search AltaVista for langergiedion syndrome Global Search - Add Url - FreeMedline - Contact Us - Search. Enter Keywords to Search and Your Choice of http://www.orthoguide.com/ortho/Langer-Giedion_Syndrome.php3
Langer=-Giedion Syndrome langergiedion syndrome. (Trichorhinophalangeal Syndrome, Type II). This Syndromecan also go under the name of langer-giedion syndrome . http://www.dickibus.co.uk/lgs.htm
Extractions: Langer-Giedion Syndrome (Trichorhinophalangeal Syndrome, Type II) This Syndrome can also go under the name of "Langer-Giedion Syndrome". A good patient's (non-jargon) description of it can be found at http://wimp.nsm.uh.edu/LGS-GD.html , and a doctor's (very jargony) description at http://wimp.nsm.uh.edu/lgs.html . The Home Page centring on LGS ican be found at http://wimp.nsm.uh.edu/LGS.htm l (University of Houston). Basically, I think (and I am not a qualified MD - in fact, I never even studied Biology at school... preferred Physics and Chemistry instead.. all 4-7 years of it!) that it occurs when one gene, or a part of it, is missing. In other words, it's a genetically based condition. It comes in two parts..... EXT1, which causes growths (benign cancers?) on bones, and another (named TRPSI by the medical/gene world) which puts a sort of a cone onto some of the growing ends of the bones. What happens when the kid grows up, and stops growing, I have yet to find out! There are other signs which some, but not all, patients have... such as being short, having folds in their skins when they're still kids (young kids, at that), and (sometimes) double-jointedness. To have one, two, or even all of these body traits is not to say "LGS", but rather that someone with LGS is more liable to also fit one or more of these descriptions.
Online And Offline Support: L langergiedion syndrome. langer-giedion syndrome Association. People servedIndividuals and families dealing with langer-giedion syndrome http://www.widesmiles.org/support/l.html
Extractions: L Langer-Giedion Syndrome Langer-Giedion Syndrome Association Louise Kinross Email address: lgsa@geocities.com Website: http://www.geocities.com/HotSprings/9308/ Laurence-Moon-Bardet-Biedl Syndrome Please note: Laurence-Moon-Bardet-Biedl Syndrome includes specific facial characteristics that do not require reconstructive surgery. The LMBBS Society (United Kingdom) Laurence Moon Bardet Biedl Syndrome (United States) People served: Families dealing with Laurence Moon Bardet Biedl Syndrome Services provided: Support and information Address: 124 Lincoln Avenue, Purchase NY 10577
Qango : Health: Diseases And Conditions: L: Langer-Giedion Syndrome langergiedion syndrome, all of Qango only this category, Options Help Home Health Diseases and Conditions L langer-giedion syndrome http://www.qango.com/dir/Health/Diseases_and_Conditions/L/Langer-Giedion_Syndrom
Extractions: WWW Medical.WebEnds.com Acrodysplasia V; Giedion-Langer Syndrome; Trichorhinophalangeal Syndrome Type II; Trichorhinophalangeal Syndrome with Exostoses; Giedion Langer Syndrome; Langer Giedion Syndrome; Syndrome, Giedion-Langer; Syndrome, Langer-Giedion Autosomal dominant disorder characterized by cone-shaped epiphyses in the hands and multiple cartilaginous exostoses Mental retardation and abnormalities of chromosome 8 are often present. The exostoses in this syndrome appear identical to those of hereditary multiple exostoses EXOSTOSES , HEREDITARY MULTIPLE).
MeSH-D Terms Associated To MeSH-C Term Langer-Giedion Syndrome MeSHD terms associated to MeSH-C term langer-giedion syndrome, G2D Home of the association of the corresponding term to langer-giedion syndrome. http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Langer-Giedion_Syndrome:unknown
OMIM Entry 150230 In a patient with langergiedion syndrome and interstitial 8q deletion, (1987) concluded that the langer-giedion syndrome is due to a deletion extending http://www.hgmp.mrc.ac.uk/cgi-bin/wrapomim?150230
OMIM Entry 190350 The langergiedion syndrome (150230), a similar disorder that includes also This is further support for the notion that the langer-giedion syndrome is http://www.hgmp.mrc.ac.uk/cgi-bin/wrapomim?190350
