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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

21. TREACHER COLLINS SYNDROME : Contact A Family - For Families With Disabled Childr
Contact a Family is a UK charity for families with disabled children. We offer information on specific conditions and rare disorders.
http://www.cafamily.org.uk/Direct/t39.html
printer friendly TREACHER COLLINS SYNDROME home how we can help medical information index of conditions ... how you can help Did you find this page
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yes no Treacher Collins syndrome: Mandibulo Dysostosis; Franceschetti-Klein It is a genetic condition characterised by malformed cheek bones, chin, nose, and jaw. Features include: drooping eyelids which may be associated with a nick in the lower lid; variable degrees of malformed or absent ears, the middle ear may also be malformed or missing causing conductive deafness; receding chin at birth; hairline and palate may also be unusual (cleft palate or choanal atresia may occur in severe cases). Associated problems may include dental, breathing and eye infections. Three similar conditions are: Nager which is a syndrome with similar mandibular dysostosis anomalies to Treacher Collins but with additional arm and digital anomalies: Aural atresia of the ears (congenital imperforation of the normal channel or pathological closure of the channel in the ears): First and second arch syndromes which are inclusive titles for developmental errors of the facial bones and which include Treacher Collins syndrome.

22. The Treacher Collins Syndrome (TCOF1) Gene Product Is Involved In
MEDICAL SCIENCES The treacher collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. World Craniofacial Foundation
treacher collins syndrome or Mandibulofacial synostosis effects the size and Children with treacher collins syndrome may have hypernasal resonance due
http://www.worldcf.org/treacher.cfm
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The World Craniofacial Foundation is dedicated to helping children and familes who experience deformities of the head and/or face by providing support and access to life-changing procedures. Reconstruct a face; create a new life. Today, we have the knowledge and technology to make these children look and feel normal. It is now possible to acheive excellent outcomes in the treatment of even the most complex craniofacial deformities. For the task ahead, support and participation is needed from all of us in order to transform the lives of those who need help.
World Craniofacial Foundation
7777 Forest Lane
Ste C-621
P.O. Box 515838
Dallas, TX 75251-5838
fax 972-566-3850
www.worldcf.org
Need Assistance? Support Groups Media Resources ... Links Treacher-Collins Syndrome Congenital Craniofacial Deformities Anatomy and Growth of the Skull Deformites of Skull Shape Non-synostic Plagiocephaly Isolated Craniosynostosis Syndromic Synostoses Apert's Syndrome Carpenter's Syndrome Crouzon's Syndrome Pfeiffer Syndrome ... Deformities of the Jaw Syndromal Facial Anomalies Hemifacial Microsomia Goldenhar Syndrome Treacher-Collins Syndrome Down's Syndrome ... Non-Syndromal Anomalies Treacher-Collins Syndrome Treacher Collins syndrome or Mandibulofacial synostosis effects the size and shape of the ears, cheek bones, and upper and lower jaws. This condition is the result of an autosomal dominant gene.

24. Treacher Collins Syndrome / Family Village Library
Synonyms Treacher CollinsFrancheschetti Syndrome; Mandibulofacial Dysostosis Web Sites * Search Google for treacher collins syndrome
http://www.familyvillage.wisc.edu/lib_trec.htm
Treacher Collins Syndrome
Synonyms: Treacher Collins-Francheschetti Syndrome; Mandibulofacial Dysostosis See Also: Deafness Craniofacial Disorders
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Treacher Collins Foundation
P.O. Box 683
Norwich, VT 05055
800-TCF-2055
Web: http://www.treachercollinsfnd.org/ The Treacher Collins Foundation aims to support, inform, and network families and individuals with Treacher Collins syndrome and related conditions; serve as a resource for current information about Treacher Collins syndrome and related conditions; provide medical, educational, and other service providers with information about Treacher Collins syndrome and related conditions and the needs of families and individuals; improve the level of understanding and acceptance by the general public of people who have facial difference; promote research activity aimed at improving the quality of life of persons with Treacher Collins Syndrome and related conditions and plan, develop, and provide services aimed at the realization of these purposes.
Where to Go to Chat with Others
  • Treacher
    To interchange feelings, concerns, issues, treatment options, etc. with families, friends of those who have Treacher Collins Syndrome (TCS).

25. Treacher Collins
treacher collins syndrome A Personal View, V OliverMacklin, tcs.london@virgin.net London, England; Tony`s Treacher Collins Page Welcome to Mirrored
http://www.kumc.edu/gec/support/treacher.html
Treacher Collins Syndrome
Treacher Collins Foundation
P.O. Box 683 Norwich, VT 05055-0683 Phone: 802-649-3050 or 1-800-TCF-2055 Executive Director: Hope Charkins, M.S.W. Web site: http://www.treachercollinsfnd.org/
The Treacher Collins Family Support Group
114 Vincent Road Thorpe Hamlet, Norwich Norfolk NR1 4HH, ENGLAND E-mail: neal@treachercollins.net Web site: http://www.treachercollins.net/
The Treacher Collins Network
Web site: http://www.geocities.com/Heartland/Plains/6153/
Personal Web Pages:
Also See:
To locate a genetic counselor or clinical geneticist in your area:

26. Cleft And Craniofacial Anomalies: Treacher Collins Syndrome
treacher collins syndrome is named after the man who described it. About half of people with treacher collins syndrome are missing some eyelashes on the
http://www.ucdmc.ucdavis.edu/children/services/cleft/health/anomalies/treacher.h
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Treacher Collins syndrome
Treacher Collins syndrome is named after the man who described it. Treacher Collins syndrome is sometimes called Mandibulofacial Dysostosis. Mandibulofacial Dysostosis describes some of the features of this syndrome. Mandibulo refers to the lower jaw, and facial to the face. Dysostosis means that certain bones are not formed normally. The lower jaw and cheekbones are often smaller than usual (also known as mandibular hypoplasia and malar hypoplasia respectively). Other possible features of Treacher Collins syndrome? Treacher Collins syndrome is associated with lower eyelid coloboma, which means a small notch missing from the lower eyelid. About half of people with Treacher Collins syndrome are missing some eyelashes on the lower eyelid. Differences in the way the ear is formed, such as absence of the external auditory canal or microtia (small ear), ear tags (extra bits of skin in front of the ear) and little pits near the ear are common. Hearing loss of varying degrees may also occur. While it is unusual to have a cleft lip and palate with Treacher Collins syndrome, cleft palate alone is not an unusual finding occurring in about a third of people with Treacher Collins syndrome. Learning problems are not normally associated with Treacher Collins syndrome.

27. Treacher Collins Family Support Group
Someone with treacher collins syndrome may have malformed cheekbones, chin, The psychological effects of treacher collins syndrome are significant due
http://www.treachercollins.net/syndrome.html

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Treacher Collins Syndrome Genetics Hearing Aids ... Email Us
Treacher Collins Syndrome The syndrome was named after an ophthalmologist called Edward Treacher Collins in 1900. It can also be known by other names such as Berry-Treacher Collins Syndrome, Franceschetti-Klein Syndrome, Franceschetti-Zwahlen Syndrome and Thomson complex. It is a condition that causes facial malformations and severe hearing loss.
Physical characteristics Someone with Treacher Collins Syndrome may have malformed cheekbones, chin, nose, jaw and temples. Eyelids are often drooping, seeming not to support the eyes, and there may be a small nick in the lower lid. The ears may be malformed or completely absent. Hairline and palate may also be unusual.
Depressed cheekbones The cheekbones can be underdeveloped or absent. This means that the c heek muscles join onto the lower jaw muscles and so cause sloping eyes. This can be corrected by surgery using implants and bone grafts.
Malformed or absent ears
This will vary greatly from case to case. Some may just have small ears; others may have no ears at all. The outer ear may be folded or squashed. The middle ear can also be malformed or missing. Any hearing loss is almost always conductive and can vary from partial to severe. Corrective surgery will depend on the individual and on which parts of the ear are missing. Artificial ears can be attached using Titanium, a metal that uniquely bonds with bone. Hearing may be improved with hearing aids. Most often a bone conduction hearing aid is used, attached to a headband, or a Bone Anchored Hearing Aid attached directly to the mastoid bone.

28. Treacher Collins Syndrome
treacher collins syndrome (Mandibulofacial Dysostosis, FranceschettiKlein Syndrome, Franceschetti Syndrome). An autosomal dominant disorder characterized
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.)

29. Cleft Palate Foundation - Treacher Collins Syndrome
Cleft Palate Foundation. CPF Publications Treacher Collins. treacher collins syndrome. What is treacher collins syndrome? treacher collins syndrome is
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?

30. Treacher Collins Syndrome | Craniofacial Center | Children's Hospital And Region
Information about Treacher Collins, a rare, inherited craniofacial condition affecting the bones, jaws, skin and muscles of the face.
http://craniofacial.seattlechildrens.org/conditions/collins.asp
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What is Treacher Collins syndrome?
Treacher Collins is a rare, inherited, congenital craniofacial condition affecting the bones, jaws, skin and muscles of the face. A syndrome is a disease or disorder that has more than one identifying feature or symptom. Children with Treacher Collins syndrome have many facial features in common, although there is a wide variation in the severity of the condition. Because this syndrome involves a number of different areas of the face, the treatment requires the skills and experience of a craniofacial team with a coordinated treatment plan. The other names for Treacher Collins syndrome are mandibulofacial dysostosis and Franceschetti-Zwalen-Klein syndrome. back to top
How much experience do you have treating Treacher Collins syndrome?

31. Treacher Collins Syndrome
treacher collins syndrome is a genetic, craniofacial birth defect which Most individuals with treacher collins syndrome have normal intelligence,
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

32. Treacher Collins Syndrome
Mandibulofacial Dysostosis Mandibulofacial Dysostosis with Limb Anomalies MFD1 Nager Acrofacial Dysostosis TCS Treacher Collins Franceschetti Treacle Gene
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Join I.B.I.S. ... Etchings Please Explore: Deafness Cleft Palate Support Groups Professional Associations ... Key Information Sources Contents include Titles above and Acrofacial Dysostosis 1 Collins Treacher Franceschetti Dysostosis, Mandibulofacial Dysostosis, Nager Acrofacial Francheschetti Klein Francheschetti, Treacher Collins Klein Francheschetti Mandibulofacial Dysostosis Mandibulofacial Dysostosis with Limb Anomalies Nager Acrofacial Dysostosis TCS Treacher Collins Franceschetti "Treacle" Gene Special Resources Treacher Collins Syndrome A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Group [Dutch] [French] [German] [Spanish] [Swedish] [Ukrainian] [*] [P] Treacher Collins Franceschetti Syndrome 1 from OMIM Gene Map Locus: 5q32-q33.1 [*] [P] Acrofacial Dysostosis 1, Nager Type

33. International Craniofacial Institute - Cleft Lip And Palate Treatment Center
treacher collins syndrome with Jaw Deformity Preoperative view of 11year-old patient with treacher collins syndrome. Postoperative lateral view 4 years
http://www.craniofacial.net/before_after/craniofacial_before_after/craniofacial_

34. International Craniofacial Institute - Cleft Lip And Palate Treatment Center
treacher collins syndrome with Jaw Deformity treacher collins syndrome with Jaw Deformity Treacher Collins with Conchal Type Microtia Treacher Collins
http://www.craniofacial.net/before_after/craniofacial_before_after/treacher_coll

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CRANIOFACIAL SYNDROME AND DEFORMITIES BEFORE AND AFTER PICTURES All Aperts Syndrome Crouzons Syndrome Down Syndrome ... Treacher Collins with External Distraction Device Treacher Collins
Preoperative frontal view of 16-year-old patient with Treacher Collins Syndrome. No previous correction had been performed. Postoperative lateral view 1 year after orthognathic surgery. Pre and postoperative lateral views of same patient.
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35. GeneReviews: Treacher Collins Syndrome
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36. Kent And Medway NHS > Treacher Collins Syndrome
Contact a Family treacher collins syndrome Link to an external website. Information and support for sufferers of treacher collins syndrome
http://www.kentandmedway.nhs.uk/disability/physical_disabilities/treacher_collin
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NATIONAL Contact a Family - Treacher Collins syndrome
Information and support for sufferers of Treacher Collins Syndrome (mandibulofacial dysostosis) and their families. Treacher Collins family support group
Offers information, support, friendship and advice to individuals and families living with Treacher Collins and similar conditions.
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37. Treacher Collins Syndrome
treacher collins syndrome Updated April 4, 2004 treacher collins syndrome Erlanger Health System, Chattanooga TN. Researched by NOAH Contributing
http://www.noah-health.org/en/genetic/conditions/treacher.html
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38. Search Result For "Treacher-Collins Syndrome"
Displaying 15 of 336. treacher collins syndrome A Guide to Understanding treacher collins syndrome; treacher collins syndrome; treacher collins syndrome
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39. Treacher Collins Syndrome
treacher collins syndrome is a rare inherited disorder characterized by distinctive abnormalities of the head and facial (craniofacial) area due to
http://www.bchealthguide.org/kbase/nord/nord647.htm
var hwPrint=1;var hwDocHWID="nord647";var hwDocTitle="Treacher Collins Syndrome";var hwRank="1";var hwSectionHWID="nord647-Header";var hwSource="en-caQ2_05";var hwDocType="Nord";
National Organization for Rare Disorders, Inc.
Treacher Collins Syndrome
Important
It is possible that the main title of the report Treacher Collins Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • Treacher Collins-Franceschetti Syndrome 1 Mandibulofacial Dysostosis Franceschetti-Zwalen-Klein Syndrome TCS
Disorder Subdivisions
  • None
General Discussion
Treacher Collins Syndrome is a rare inherited disorder characterized by distinctive abnormalities of the head and facial (craniofacial) area due to underdevelopment (hypoplasia) of certain portions of the skull (e.g., supraorbital rims and zygomatic arches). Although the symptoms and physical characteristics associated with Treacher Collins Syndrome can vary greatly in severity from patient to patient, craniofacial abnormalities tend to involve the cheekbones, jaws, mouth, ears, and/or eyes.
Resources
Treacher Collins Foundation
P.O. Box 683

40. Treacher Collins Syndrome - [Support Group]
This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a
http://www.bchealthguide.org/kbase/shc/shc29tre.htm
var hwPrint=1;var hwDocHWID="shc29tre";var hwDocTitle="Treacher Collins Syndrome";var hwRank="1";var hwSectionHWID="shc29tre-Header";var hwSource="en-caQ2_05";var hwDocType="Shc";
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Treacher Collins Syndrome
This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
Treacher Collins Foundation
National network. Founded 1988
Support for families, individuals and professionals re: Treacher Collins syndrome and related disorders. Provides networking, educational materials, newsletter, information and referrals, phone support, resource list, bibliography and central library, videos and booklets. Online resources and newsletter.
WRITE:
Treacher Collins Fdn.
P.O. Box 683
Norwich, VT 05055
E-MAIL: hopecharkins@hotmail.com

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