Extractions: This Article Abstract Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Isaac, C. Articles by Meier, U. T. Vol. 11, Issue 9, 3061-3071, September 2000 Cynthia Isaac, Karen L. Marsh, William A. Paznekas, Jill Dixon, Michael J. Dixon, Ethylin Wang Jabs, and U. Thomas Meier Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461; School of Biological Sciences and Departments of Dental Medicine and Surgery, University of Manchester, Manchester M13 9PT, United Kingdom; and Center for Craniofacial Development and Disorders, McKusick-Nathans Institute of Genetic Medicine, Departments of Pediatrics, Medicine, and Plastic Surgery, The Johns Hopkins University School of Medicine Baltimore, Maryland 21287 Submitted May 9, 2000; Revised June 19, 2000; Accepted June 26, 2000
Extractions: This Article Full Text Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Isaac, C. Articles by Meier, U. T. Vol. 11, Issue 9, 3061-3071, September 2000 Cynthia Isaac, Karen L. Marsh, William A. Paznekas, Jill Dixon, Michael J. Dixon, Ethylin Wang Jabs, and U. Thomas Meier Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461; School of Biological Sciences and Departments of Dental Medicine and Surgery, University of Manchester, Manchester M13 9PT, United Kingdom; and Center for Craniofacial Development and Disorders, McKusick-Nathans Institute of Genetic Medicine, Departments of Pediatrics, Medicine, and Plastic Surgery, The Johns Hopkins University School of Medicine Baltimore, Maryland 21287 Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development caused by mutations in the gene . Its gene product, treacle, consists mainly of a central
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 ... Cited by other online articles PubMed PubMed Citation Articles by Edwards, S. J. Articles by Dixon, M. J. Journal of Medical Genetics, 1996, Vol 33, 603-606 SJ Edwards, A Fowlie, MP Cust, DT Liu, ID Young and MJ Dixon
Treacher Collins Connection Mission To build a community of people with treacher collins syndrome and their Treacher Collins treacher collins syndrome is a genetic craniofacial http://www.tcconnection.org/aboutus.html
Extractions: Mission : To build a community of people with Treacher Collins syndrome and their families in an environment that transforms people through face to face sharing of stories, surgeries, pictures, heartaches, and love. Tre acher Collins: Treacher Collins syndrome is a genetic craniofacial syndrome that is characterized by a range of distinctive facial anomalies. The main characteristics of TCS are downward slanting eyes, small lower jaw, and malformed or missing ears. These anomalies cause hearing, breathing, and eating problems. Individuals and families also struggle with the psychological aspects of having a facial difference. About 1 in every 10,000 babies is born with TCS. For more information about Treacher Collins syndrome and to view personal experiences of people with TCS, please visit www.treachercollins.org Vision : Each event is essential in many ways; not only is it important for people with TCS to meet others like them, it is equally important to network about medical doctors, procedures, and hospitals. The TCC will organize at least one yearly event to bring together those with TCS and their families. History Five volunteers founded the TCC in 2001 as a result of successfully organizing the first TCS retreat. Over 65 people attended the first retreat and as a result, we will now have an annual TCS retreat. Over 100 people attended our 2002 TCS retreat on June 28-30 in Columbia, MD.
Extractions: Vol. 105 No. 3, March 1979 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager Articles in PubMed by Shprintzen RJ Rakoff SJ Contact me when this article is cited R. J. Shprintzen, C. Croft, M. D. Berkman and S. J. Rakoff Examination of 11 patients with Treacher Collins syndrome (TCS), with the use of multiple-view videofluoroscopy and nasopharyngoscopy of the pharynx, disclosed marked narrowing of the airway. In several patients, the pharynx was less than 1 cm in width at its most narrow point. It is thought that reduced airway in TCS may help to explain the frequent reports of neonatal death associated with the syndrome. Pharyngeal narrowing was found
MedlinePlus Medical Encyclopedia: Treacher-Collins Syndrome treachercollins syndrome is a hereditary condition that causes facial defects. treacher-collins syndrome is inherited as an autosomal dominant trait. http://www.nlm.nih.gov/medlineplus/ency/article/001659.htm
Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Alternative names Mandibulofacial dysostosis Definition Return to top Treacher-Collins syndrome is a hereditary condition that causes facial defects. Causes, incidence, and risk factors Return to top Treacher-Collins syndrome is inherited as an autosomal dominant trait. More than half of all cases are thought to be new mutations because there is no family history of the disease. A defective gene, called treacle, is the cause of this disease. This condition has variable expression, which means there may be a great variation in severity from generation to generation. Symptoms Return to top Signs and tests Return to top The child usually will show normal intelligence. Examination of the infant can show various abnormalities, including:
► Treacher-Collins Syndrome A medical encycopedia article on the topic treacher-collins syndrome. http://www.umm.edu/ency/article/001659.htm
Extractions: Causes, incidence, and risk factors: Treacher-Collins syndrome is inherited as an autosomal dominant trait. More than half of all cases are thought to be new mutations because there is no family history of the disease. A defective gene, called treacle, is the cause of this disease. This condition has variable expression, which means there may be a great variation in severity from generation to generation.
Treacher-Collins' Syndrome, Vanderbilt Craniofacial Treatment Center treacher collins syndrome, VUMC Med Art Group. treachercollins syndrome. treacher-collinsÂ’ syndrome is characterized by lack of bone development in the http://surgery.vanderbilt.edu/surgery/plastic/cfa/treacher.htm
AllRefer Health - Treacher-Collins Syndrome (Mandibulofacial Dysostosis) treachercollins syndrome (Mandibulofacial Dysostosis) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors http://health.allrefer.com/health/treacher-collins-syndrome-info.html
Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Go To Main Page Alternate Names : Mandibulofacial Dysostosis Definition Treacher-Collins syndrome is a hereditary condition that causes facial defects. Treacher-Collins syndrome is inherited as an autosomal dominant trait. More than half of all cases are thought to be new mutations because there is no family history of the disease. A defective gene, called treacle, is the cause of this disease. This condition has variable expression, which means there may be a great variation in severity from generation to generation.
Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia
Extractions: Advanced Search Or click the first letter of a drug name: A B C D ... Z Injury Disease Nutrition Poison ... Z Treacher-Collins syndrome is a hereditary condition that causes facial defects. Mandibulofacial dysostosis Treacher-Collins syndrome is inherited as an autosomal dominant trait. More than half of all cases are thought to be new mutations because there is no family history of the disease. A defective gene, called treacle, is the cause of this disease. This condition has variable expression, which means there may be a great variation in severity from generation to generation. The child usually will show normal intelligence. Examination of the infant can show various abnormalities, including:
Extractions: Causes, incidence, and risk factors: Treacher-Collins syndrome is inherited as an autosomal dominant trait. More than half of all cases are thought to be new mutations because there is no family history of the disease. A defective gene, called treacle, is the cause of this disease. This condition has variable expression, which means there may be a great variation in severity from generation to generation.
Definition Of Treacher-Collins Syndrome - EarSurgery.com treachercollins syndrome A developmental complex in which the afflicted usually has underdeveloped cheek bones, a downward slant of the eyes, a small chin, http://www.earsurgery.com/content/glossary/treacher-collinssyndrome.html
Extractions: For Researchers For Librarians Authors: Source: Annals of Allergy, Asthma and Immunology , Volume 80, Number 1, January 1998, pp. 50-54(5) Publisher: View Table of Contents full text options Abstract: Background: Treacher-Collins syndrome, an autosomal dominantly inherited malformation of structures derived from the first and second branchial arch, has an incidence of 1:10,000 newborns. The prevalence of dermatomyositis at less than 24 years of age has been estimated at 1 per 100,000. The occurrence of both Treacher-Collins syndrome and dermatomyositis combined in the same patient should occur once in every 1,000,000 subjects. Methods: We report a patient with Treacher-Collins syndrome who developed dermatomyositis at the age of 5 years.
Weyers' Syndrome II (www.whonamedit.com) Miller s syndrome NagerDe Reynier syndrome treacher collins syndrome treacher collins syndrome, or mandibulofacial dysostosis syndrome, is entered as http://www.whonamedit.com/synd.cfm/2001.html
Extractions: 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 syndrome present from birth, affecting both sexes, characterised by postaxial polydactyly of the hands and feet, hexadactyly and fusion of 5th and 6th metatarsals and metacarpals, and bony clefts of the mandibular symphysis. Other features include anomalies of lower incisors and oral vestibule, ear anthelices, hypoplastic and dysplastic nails, and mild shortness of stature. Inheritance is autosomal dominant with variable expression.
Treacher-Collins Syndrome Federally Funded Research on treachercollins syndrome. The National Library of Medicine PubMed Academic Periodicals covering treacher-collins syndrome http://www.icongrouponline.com/health/Treacher-Collins_Syndrome_Ph.html
Extractions: E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis In March 2001, the National Institutes of Health issued the following warning: "The number of Web sites offering health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading." Furthermore, because of the rapid increase in Internet-based information, many hours can be wasted searching, selecting, and printing. Since only the smallest fraction of information dealing with Treacher-Collins syndrome is indexed in search engines, such as www.google.com or others, a non-systematic approach to Internet research can be not only time consuming, but also incomplete. This book was created for medical professionals, students, and members of the general public who want to conduct medical research using the most advanced tools available and spending the least amount of time doing so. Related Conditions/Synonyms Franceschetti-Zwalen-Klein syndrome; mandibulofacial dysostosis; Treacher-Collins-Franceschetti syndrome 1
Dr. Koop - Treacher-Collins Syndrome treachercollins syndrome is a hereditary condition that causes facial defects. http://www.drkoop.com/ency/93/001659prv.html
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Treacher-Collins Syndrome treachercollins syndrome is a hereditary condition that causes facial defects. http://adam.about.com/encyclopedia/001659trt.htm
Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zCMt='a00' About Healthcare Center Healthcare Center Essentials ... Surgeries and Procedures zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Allergies Arthritis Asthma Breast Cancer ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/7.htm','');w(xb+xb); Search Healthcare Center ENCYCLOPEDIA INDEX Injury Disease Nutrition Poison ... Z Overview Symptoms Treatment Prevention Alternative Names: Mandibulofacial dysostosis Treatment: Treatment consists of testing for and treating any hearing loss so a child can perform up to normal level in school. Plastic surgery can address the receding chin and other defects. Support Groups: Treacher Collins Foundation Expectations (prognosis): Children with Treacher-Collins should grow to become normally functioning adults of normal intelligence. Careful attention to any hearing problems helps ensure better performance in school. Complications: Calling your health care provider: This condition is usually apparent at birth. Call your health care provider if you have a child with Treacher-Collins syndrome and the hearing appears to be worse, or if other problems arise. A good plastic surgeon is very important as there is sometimes a need for a series of operations over years to correct birth defects.
