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         Treacher Collins Syndrome:     more detail
  1. Treacher Collins Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  2. Treacher Collins syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amie, MS Stanley, 2005

41. Health Library -
treacher collins syndrome. Important It is possible that the main title of the report treacher collins syndrome is not the name you expected.
http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

42. Treacher Collins Syndrome
Submit Your Site to the treacher collins syndrome category. Submit Your Site to the treacher collins syndrome category. Sponsored Results. Health Spotlight.
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43. Cleft Palate Foundation - Treacher Collins Syndrome
treacher collins syndrome. What is treacher collins syndrome? Remember that children with treacher collins syndrome, like all other children, are individuals.
http://www.cleftline.org/publications/treacherCollins.htm
Cleft Palate Foundation Publications Cleft Palate Foundation CPF Publications : Treacher Collins
Treacher Collins Syndrome
What is Treacher Collins Syndrome?
Treacher Collins syndrome is the name given to a birth defect which may affect the size and shape of the ears, eyelids, cheek bones, and upper and lower jaws. The extent of facial deformity varies from one affected individual to another. A physician named Treacher Collins was one of the first to describe this birth defect. "Syndrome" refers to the group of deformities which characterizes affected individuals. Another commonly used medical name for this syndrome is "mandibulofacial dysostosis." What causes it?
This syndrome is caused by an abnormality in the genes. If both parents are normal, that is showing no signs of the syndrome themselves, this abnormality is the result of a change in the genetic material at the time of conception. The exact cause of this change is not known. If one parent is affected, the abnormal gene is then known to have been contributed by that parent. Does this mean that this can happen again in my family?

44. Craniofacial Center | Dallas, Texas
treacher collins syndrome has been shown to occur with the same frequency in boys and girls. Currently, no one knows what causes this condition to occur.
http://www.thecraniofacialcenter.org/treachercollins.html

Treacher Collins Sydrome:
Overview:
Physical Traits
Treatment

45. TREACHER COLLINS SYNDROME (MANDIBULOFACIAL DYSOSTOSIS)
Features Listed For treacher collins syndrome (MANDIBULOFACIAL DYSOSTOSIS). McKusick 154500. Absent auditory canal; Anal atresia/stenosis;
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1715

46. Treacher Collins Syndrome
treacher collins syndrome. Most individuals with treacher collins syndrome have normal intelligence, and are therefore able to attend regular schools.
http://mick.murraystate.edu/cdi684/cdi684001/LBROWN/
Treacher Collins Syndrome
"I hope to melt away the uncertainty surrounding Treacher Collins Syndrome in
hopes that a new trend in society will arise- a trend that looks inside the soul before
judging someone because they don't look normal." - Annie

Overview
Treacher Collins Syndrome is a genetic, craniofacial birth defect which primarily affects the size and shape of the ears, eyelids, cheek bones, and upper and lower jaws. It occurs in approximately 1 of 10,000 births, making it a rare condition. The extent of severity varies from one affected individual to another. Some individuals have very subtle features of this syndrome that may go unrecognized, while others manifest more severe features that are noticed immediately. Most individuals with Treacher Collins Syndrome have normal intelligence, and are therefore able to attend regular schools. No evidence has been found that these individuals have a lower life expectancy than those who are not affected by the syndrome. Alternative medical names for this syndrome include "Mandibulofacial Dysostosis" and "Franceschetti- Klein Syndrome". Created by: Laura Brown, CDI 684: Craniofacial Anomalies

47. :: Ez2Find :: Treacher Collins Syndrome
Guide treacher collins syndrome, Global Metasearch Any Language Guides, treacher collins syndrome. ez2Find Home Directory Health
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48. TREACHER COLLINS SYNDROME
Terms of Use. treacher collins syndrome. Frequency of Internet Expressions treacher collins syndrome. Top. Modern Translation treacher collins syndrome.
http://www.websters-online-dictionary.org/definition/english/Tr/Treacher Collins
Philip M. Parker, INSEAD.
TREACHER COLLINS SYNDROME
Frequency of Internet Keywords: TREACHER COLLINS SYNDROME
The following statistics estimate the number of searches per day across the major English-language search engines as identified by various trade publications. Hyperlinks lead to commercial use of the expression at Amazon.com
Expression Frequency
per Day
treacher collins syndrome
Source: compiled by the editor from various references ; see credits. Top
Modern Translation: TREACHER COLLINS SYNDROME
Language Translations for "TREACHER COLLINS SYNDROME"; alternative meanings/domain in parentheses.
Danish
Franceschetti's syndrom (Franceschetti syndrome, Franceschetti-Zwahlen syndrome, mandibulofacial dysostosis, recidivating erosion of the cornea, recurring erosion of the cornea), Dysostosis mandibulofacialis (Franceschetti syndrome, Franceschetti-Klein syndrome, Franceschetti's syndrome, Franceschetti-Zwahlen syndrome, mandibulofacial dysostosis, Treacher-Collins syndrome). ( various references
Dutch
syndroom van Franceschetti (Franceschetti syndrome, Franceschetti's syndrome, Franceschetti-Zwahlen syndrome, mandibulofacial dysostosis, recidivating erosion of the cornea, recurring erosion of the cornea)

49. Characterization Of The Treacher Collins Syndrome Gene
Characterization of the treacher collins syndrome Gene. Keywords. Craniofactal; treacher collins syndrome; Nucleolar phosphoptotein; Development; Mouse model.
http://www.vipbg.vcu.edu/hg/grant/DE13172.shtml
D epartment of H uman G enetics Projects
Characterization of the Treacher Collins Syndrome Gene
National Institutes of Health
Grant number
Principal Investigator:
Rita Shiang Co-investigators:
Years:
Abstract
Keywords
  • Craniofactal
  • Treacher Collins syndrome
  • Nucleolar phosphoptotein
  • Development
  • Mouse model
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Questions, comments, suggestions, problems? Contact the Webmaster Date last modified: August 27, 2001

50. In Vivo And In Vitro Models Of Treacher Collins Syndrome
In vivo and in vitro models of treacher collins syndrome. Jeffress Craniofactal; treacher collins syndrome; Nucleolar phosphoptotein; Development; Mouse model.
http://www.vipbg.vcu.edu/hg/grant/ShiangJ566.shtml
D epartment of H uman G enetics Projects
In vivo and in vitro models of Treacher Collins Syndrome
Jeffress
Grant number
Principal Investigator:
Rita Shiang Co-investigators:
Years:
Abstract
Keywords
  • Craniofactal
  • Treacher Collins syndrome
  • Nucleolar phosphoptotein
  • Development
  • Mouse model
information mission history relations contact ... highlights research facilities projects collaborations publications people faculty students staff directory ... jobs education seminars graduate courses graduate program Home
Questions, comments, suggestions, problems? Contact the Webmaster Date last modified: August 27, 2001

51. A To Z Encyclopedia Topic: Treacher Collins Syndrome
Craniofacial Anomalies Programs. Unfortunately, at this time, we are not able to provide information about this condition or procedure.
http://web1.tch.harvard.edu/cfapps/A2ZtopicDisplay.cfm?Topic=Treacher Collins Sy

52. Treacher Collins Syndrome
Maxiollofacial Pathology. treacher collins syndrome (Mandibulofacial Dysostosis, FranceschettiKlein Syndrome, Franceschetti Syndrome). An
http://www.dental.mu.edu/oralpath/lesions/treachercollins/treachercollins.htm
Treacher Collins Syndrome
(Mandibulofacial Dysostosis, Franceschetti-Klein Syndrome, Franceschetti Syndrome)
An autosomal dominant disorder characterized by certain facial features including downward slanting palpebral fissures, sunken cheekbones, receding chin, and malformed ears.
Clinical Features: newborn no gender predilection sunken or depressed cheekbones downward sloping lower eyelids receding chin and narrow face severe mandibular hypoplasia possible unilateral or bilateral macrostomia , projection of scalp hair onto the lateral cheek, visual loss, external ear canal defect, hearing loss, and cleft palate possible widely-spaced, hypoplastic and / or displaced teeth Radiographic Features: mandibular hypoplasia hypoplasia of the zygomatic arch peaked bony nasal contour Etiology: genetic Tissue of Origin: embryonic tissue Main Pathologic Process: developmental Treatment: genetic counseling treat the anomalies associated with this syndrome orthodontic treatment surgery for functional and cosmetic reasons Prognosis: varies by the severity of the clinical manifestations (respiratory difficulties, feeding and swallowing difficulties, deafness, loss of vision, etc.)

53. Treacher Collins Syndrome
Ailment Name treacher collins syndrome. Join this Community get help by emailing and chatting to others, and sharing information and experiences,
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54. Treacher Collins Syndrome
The New Health Directory, Directory, Home Health Support Groups Conditions and Diseases Facial Differences treacher collins syndrome (5) See Also
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55. Increased Fistula Risk Following Palatoplasty In Treacher Collins Syndrome
Journal Vol. 40, No. 3, pp. 280–283. Increased Fistula Risk Following Palatoplasty in treacher collins syndrome. Stephen Bresnick
http://apt.allenpress.com/aptonline/?request=get-abstract&issn=1545-1569&volume=

56. Parent Seeks To Raise Awareness Of Treacher Collins Syndrome -- January 3, 2003
Parent seeks to raise awareness of treacher collins syndrome Friday January 3, 2003 M. Strutzenberger Ever since her son was born two years ago with the
http://www.familynet.on.ca/News/Dec_02/jan3.htm
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Parent seeks to raise awareness of Treacher Collins Syndrome
Friday January 3, 2003 M. Strutzenberger
Ever since her son was born two years ago with the condition, Christina Goldman has been amazed by the lack of resources, support for and information about Treacher Collins Syndrome in Canada. "There's absolutely nothing in Canada," she says. "Not even a database on how to get in contact with the right physicians. We don't have anything with families who've had experience with the syndrome, no success stories. We don't even have data on how many people have Treacher Collins, or what complications there might be or how to deal with them…" Christina believes there is a real need get the word out about Treacher Collins
and is actively seeking to raise awareness of both the syndrome and related medical issues such as tracheostomy, g-tube feeds, and surgeries. "There are so many who have medical related issues who need an advocate in my area alone," she says.

57. Treacher Collins Syndrome - HUM-MOLGEN
Author, Topic treacher collins syndrome. After searching the TreacherCollins syndrome in the Rare diseases data base (www.orpha.net), I came up with a lab.
http://www.hum-molgen.de/bb/Forum2/HTML/000120.html

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Treacher Collins Syndrome
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register preferences faq ... next oldest topic Author Topic: Treacher Collins Syndrome Administrator
Administrator posted 12-10-2002 02:45 PM Dear Sirs
We have a couple who have a son with Treachar Collins Syndrome, and they want have more children. Therefore, I would like to know if you can help me to find the Laboratory which performs the molecular diagnosis of this condition. Thank you in advance
Yours sincerely
MT Lourenço MD
Seerviço de Genética Médica
Hospital Egas Moniz 1300 Lisboa-PORTUGAL e-mail addres:terjea@mail.telepac.pt or genclin@hegasmoniz.min-saude.pt IP: 160.45.191.21 Member posted 12-17-2002 04:50 PM After searching the Treacher-Collins syndrome in the Rare diseases data base (www.orpha.net), I came up with a lab. in Rome that does the diagnose you formerly refered to: Person(s) responsible: Sig Dr Mario BENGALA Sig Pr Giuseppe NOVELLI Name of the service: Laboratorio di Genetica Medica - Dipartimento di Biopatologia e Diagnostica per Address : Università degli Studi "Tor Vergata" Via Montpellier 1 00133 ROMA ITALIA Phone : Fax : I hope to have been helpful in this matter.

58. Pseudo-Treacher Collins Syndrome - HUM-MOLGEN
Author, Topic Pseudotreacher collins syndrome. They had been diagnosed as having treacher collins syndrome, but that clearly is not the correct diagnosis.
http://www.hum-molgen.de/bb/Forum2/HTML/000017.html

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Pseudo-Treacher Collins syndrome
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register preferences faq ... next oldest topic Author Topic: Pseudo-Treacher Collins syndrome Administrator
Administrator posted 01-27-2000 10:23 AM We have recently seen a family in which the combination of apparent
branchial arch anomalies and minor digital defects is inherited as an
autosomal dominant trait. They had been diagnosed as having Treacher
Collins syndrome, but that clearly is not the correct diagnosis. They are
very motivated to have someone try to identify the gene. There are at least
6 affected individuals in three generations. Please contact: Helga Toriello, Ph.D. Genetics Services 21 Michigan St. Suite 465 Grand Rapids, MI 49503 phone: 616-391-2701 fax: 616-391-3114 Email: helga.toriello@spectrum-health.org IP: 160.45.191.21 All times are ET (US) next newest topic next oldest topic Administrative Options: Close Topic Archive/Move Delete Topic Hop to: Select a Forum or Archive List of Forums: Biotechnical requests and sources DIAGnostics - Clinical Research (professional requests) Ethical, legal and social implications

59. Health Library -
treacher collins syndrome. Founded 1988Support for families, individuals and professionals re treacher collins syndrome and related disorders.
http://12.31.13.113/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29tre

60. EUROCRAN: Treacher Collins Syndrome
Directory of European Resources Patient Support Groups Syndrome specific support groups treacher collins syndrome. treacher collins syndrome
http://www.eurocran.org/content.asp?contentID=1320

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