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         Langer-giedion Syndrome:     more detail

1. Index
International network of families and professionals providing information and support to people affected by langergiedion syndrome.
http://www.geocities.com/HotSprings/9308/
This page hosted by Get your own Free Home Page We have moved to... http://lgsa.net Please visit us in our new home!

2. Langer-Giedion Syndrome
langergiedion syndrome Contains detailed information and links to various resources . Langer Giedion Syndrome Association Contains information on LGSA,
http://wimp.nsm.uh.edu/LGS.html
The University of Houston
TRPSII/LGS Homepage
Maps TRPS I TRPSII/LGS TRPS III/SKS ... Feedback This page is an attempt consolidate information and resources relevant to Tricho-Rhino-Phalangeal Syndrome Type II, also known as Langer-Giedion Syndrome. I eventually hope it will be a site that research scientists, clinicians, M.D.'s as well as affected individuals and families and friends of affected individuals will find useful. It will be upated and improved as often as possible.
Links to the Online Mendelian Inheritance of Man (OMIM)
Reference Links
General Information for the Non-Scientist

3. Langer-Giedion Syndrome
The University of Houston Langer Giedion Syndrome home page. Information and resources for professionals and families.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. TRPSII References
Published manuscripts on Langer Giedion Syndrome with links to the NCBI PubMed (1999) Genes and chromosomal breakpoints in the langergiedion syndrome
http://wimp.nsm.uh.edu/LGS-ref.html
The Wells Lab
LGS/TRPS II Reference Page.
Published manuscripts on Langer Giedion Syndrome with links to the NCBI PubMed Database. Last updated 9/03.
  • Hilton et al. (2002) Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes. J Hum Genet.
  • Wuyts et al. (2002) Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion. Am J Med Genet.
  • Feely et al. (2002) Cytogenetic and molecular cytogenetic evidence of recurrent 8q24.1 loss in osteochondroma.. Cancer Genet Cytogenet.
  • Shin and Chang (2001) Trichorhinophalangeal syndrome, type II (Langer-Giedion syndrome). Dermatol Online J.
  • Gassel et al. (2001) Orthopedic considerations of trichorhinophalangeal syndrome type II Klin Padiatr. 213: 334-7. [Article in German]
  • Batania et al. (2001) Familial deletion of (8)(q24.13q24.22) associated with a normal phenotype. Clin Genet.
  • Wakui and Fukushima (2001) Tricho-rhino-phalangeal syndrome, type II Ryoikibetsu Shokogun Shirizu.

5. Langer-Giedion Syndrome
The University of Houston Langer Giedion Syndrome home page. Information and resources for professionals and families.
http://wimp.nsm.uh.edu/lgs.html
The University of Houston
TRPSII/LGS Homepage
Maps TRPS I TRPSII/LGS TRPS III/SKS ... Feedback This page is an attempt consolidate information and resources relevant to Tricho-Rhino-Phalangeal Syndrome Type II, also known as Langer-Giedion Syndrome. I eventually hope it will be a site that research scientists, clinicians, M.D.'s as well as affected individuals and families and friends of affected individuals will find useful. It will be upated and improved as often as possible.
Links to the Online Mendelian Inheritance of Man (OMIM)
Reference Links
General Information for the Non-Scientist

6. Langer-Giedion Syndrome Association
International network of families and professionals providing information and support to people affected by langergiedion syndrome.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

7. Rozenberg Family
The langergiedion syndrome Association supports families affected by theTrichorhinophalangeal Syndromes (I, II, III) and works with medical specialists
http://lgsa.net/
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Welcome to our family site. Here you can keep updated on our family and learn about Ariel and the syndrome that affects her, Langer-Giedion Syndrome.
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Look at our online photo album filled with pictures of our vacations, and family events. Trichorhinophalangeal Syndrome Association on YAHOO Health Chromosome Deletion Outreach ... Our Kids This site was last updated

8. Langer-Giedion Syndrome (www.whonamedit.com)
langergiedion syndrome Syndrome characterized by a combination of mental retardation and a long list of physical abnormalities, including multiple
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. LGS Description
Houston langergiedion syndrome (Trichorhinophalangeal Syndrome, Type II) isa rare Published in LINKS - A Publication of the langer-giedion syndrome
http://lgsa.net/lgs description.htm

10. Langer Giedion Syndrome Association
The langergiedion syndrome Association supports families affected by the Trichorhinophalangeal Syndromes (I, II, III) and works with medical
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

11. LGS Description
Just what is langergiedion syndrome? By Dan Wells, PhD. Houston langer-giedion syndrome (Trichorhinophalangeal Syndrome, Type II) is a rare
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. Langer-Giedion Syndrome (www.whonamedit.com)
langergiedion syndrome Syndrome characterized by a combination of mentalretardation and a long list of physical abnormalities, including multiple extoses
http://www.whonamedit.com/synd.cfm/1865.html

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Whonamedit.com does not give medical advice.
This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor.
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Langer-Giedion syndrome Also known as: Alè-Calò syndrome Klingmüller’s syndrome Synonyms: Acrodysplasia V syndrome, acrodysplasia dysostoses syndrome, trichorhinophalangeal dysplasia syndrome type II, multiple exostoses-mental retardation (MEMR) syndrome, trichorhino-auriculophalangeal multiple extoses (TRAMPE) dysplasia. Associated persons: G. Alè S. Calò Andreas Giedion Viktor Felix Karl Klingmüller ... Leonard O. Langer Jr. Description: Syndrome characterized by a combination of mental retardation and a long list of physical abnormalities, including multiple extoses, peculiar facies, and loose redundant skin. Facial features include a bulbous nose with thickened septum and alae, wide prominent philtrum, thin upper lips, and small mandible. During first five years of life recurrent respiratory infections. One of the contiguous gene syndromes. Present from birth. Both sexes affected. Bibliography:
  • G. Alè, S. Calò:

13. Langer Giedion Syndrome
langergiedion syndrome (also known as Trichorhinophalangeal Syndrome, Type II) is a multi-system disorder involving the deletion of at least two
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. Www.whonamedit.com
Klingmüller’s syndrome (langergiedion syndrome) langer-giedion syndrome.Syndrome characterized by a combination of mental retardation and a long list
http://www.whonamedit.com/syndlist.cfm/193

Home

List categories

Eponyms A-Z

Biographies by country
...
Contact

Whonamedit.com does not give medical advice.
This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor.
A recommendation:
Hypography
is an open community about science and all things related
Eponyms in category: Multiple congenital anomalies 189 main and alternative entries found. Aase-Smith syndrome A familial deformity syndrome. Aase’s syndrome (Aase-Smith syndrome) A familial deformity syndrome. Alè-Calò syndrome (Langer-Giedion syndrome) Syndrome characterized by a combination of mental retardation and a long list of physical abnormalities, including multiple extoses, peculiar facies, and loose redundant skin. Alfi's syndrome A very rare chromosome anomaly also known as monosomy 9P. Aniridia-Wilms' tumor association (Brusa-Torricelli syndrome) A congenital syndrome in which aniridia and nephroblastoma (Wilms' tumour) is associated with multiple abnormalities.

15. Langer=-Giedion Syndrome
langergiedion syndrome
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

16. Langer Giedion Syndrome
langergiedion syndrome Association 89 Ingham Ave. langer-giedion syndrome (alsoknown as Trichorhinophalangeal Syndrome, Type II) is a multi-system
http://www.kumc.edu/gec/support/langer_g.html
Langer-Giedion Syndrome (also Trichorhinophalangeal Syndrome, Type II or Type I)
Langer-Giedion Syndrome
Langer-Giedion Syndrome Association
89 Ingham Ave. Toronto, ON M4K 2W8 Canada e-mail: kinross@istar.ca Langer-Giedion Syndrome (also known as Trichorhinophalangeal Syndrome, Type II) is a multi-system disorder involving the deletion of at least two genes on the long arm of chromosome 8 (8q24.11). In 1997, this international organization founded for people affected by LGS and Trichorhinophalangeal Syndrome, Type I (a milder condition). Includes over 30 families from around the world affected by LGS, and more than 10 affected by TRPSI.
Langer-Gideon Syndrome Association - TRPS (all types)
c/o Raquel Rozenberg 11695 Boulton Ave. San Diego, CA 92128 E-mail: lgsa@geocities.com
Langer Giedion Syndrome , Wells Lab
Also See:
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17. Trichorhinophalangeal Syndrome, Type II (Langer-Giedion Syndrome)
Trichorhinophalangeal Syndrome, Type II (langergiedion syndrome) Helen T Shin and Mary Wu Chang Dermatology Online Journal 7(2) 8
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. HONselect - Langer-Giedion Syndrome
Translate this page Giedion Langer Syndrome - Langer Giedion Syndrome. Français, Langer-Giedion,syndrome, - Acrodysplasie V - Dysplasie tricho-phalangienne type II
http://www.hon.ch/HONselect/RareDiseases/C05.116.099.708.582.html
List of rare diseases: English Deutsch
Language:
MeSH term:
Accepted terms:
English: Langer-Giedion Syndrome - Acrodysplasia V
- Giedion-Langer Syndrome
- Trichorhinophalangeal Syndrome Type II
- Trichorhinophalangeal Syndrome with Exostoses
- Giedion Langer Syndrome
- Langer Giedion Syndrome
Français: Langer-Giedion, syndrome - Acrodysplasie V - Dysplasie tricho-phalangienne type II - Syndrome Langier-Giedion Deutsch: Langer-Giedion-Syndrom - Akrodysplasie V - Giedion-Langer-Syndrom - Tricho-rhino-phalangeale Dysplasie Typ II Español: Síndrome de Langer-Giedion - Acrodisplasia V - Síndrome Tricorrinofalangiano Tipo II - Síndrome de Giedion-Langer Português: Síndrome de Langer-Giedion - Acrodisplasia V - Síndrome Tricorrinofalangeana Tipo II - Síndrome de Giedion-Langer HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: No Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C05.116.099.708.582.html Last modified: Wed May 18 2005

19. Langer-Giedion, Syndrome Sites Et Documents Francophones
Syndrome LangierGiedion . Arborescence(s) du thesaurus MeSH contenant le mot-cl Langer-Giedion, syndrome langer-giedion syndrome
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

20. Langer-Giedion Syndrome - Acrodysplasia V - Information Page With HONselect
Autosomal dominant disorder characterized by coneshaped epiphyses in the hands
http://www.hon.ch/HONselect/RareDiseases/EN/C05.116.099.708.582.html
InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese
the word the part of word in MeSH term in MeSH term and description Information on "Langer-Giedion Syndrome": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese
Langer-Giedion Syndrome Definition: 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
Synonym(s): Acrodysplasia V / Giedion-Langer Syndrome / Trichorhinophalangeal Syndrome Type II / Trichorhinophalangeal Syndrome with Exostoses /
See Related: Exostoses, Multiple Hereditary
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Web resources for "Langer-Giedion Syndrome" English French = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: HONcode - NORD - National Organization for Rare Disorders, Inc.

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