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         Sticklers Syndrome:     more detail
  1. Stickler Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  2. Stickler syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Jennifer, MS Wilson, 2005
  3. Cleft Lip and Palate: Congenital disorder, Paul Tessier, Orbicularis oris muscle, Craniofacial team, Palatine uvula, Clefting prevalence in different cultures, ... syndrome, Stickler syndrome, Ralph Millard
  4. Stickler: the Elusive Syndrome by Wendy L. Hughes, 2006-11

21. Craniofacial Forum - View Questions
Recent Questions. sticklers syndrome (eyes) By Amy Feldman Lewanda, MD (06May-2004).Enzyme build up in cornea in stickler syndrome in twenty year old.
http://qa.hopkins-aids.edu/forum/view_question.html?section_id=321&id=84417&cate

22. Craniofacial Forum - Email To A Friend/Colleague
sticklers syndrome (eyes) By Amy Feldman Lewanda, MD (06May-2004).Enzyme build up in cornea in stickler syndrome in twenty year old.
http://qa.hopkins-aids.edu/forum/email_to_friend.html?id=84417&cat_id=0§ion_

23. Stickler - Marshall Syndrome
Special Resources SOS Ask experts or consultants for information SticklerSyndrome. Several facial features are common with sticklers syndrome.
http://ibis-birthdefects.org/start/sticksyn.htm
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... Etchings Please Explore: 11 / 22 Translocation Cleft Lip Pierre Robin S. Cleft Palate ... Key Information Sources Topics include Titles and Stickler S. Type I - II - III Special Resources Stickler Syndrome A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Group [Ukrainian] Stickler Syndrome by Nathaniel H Robin, MD et al. from GENE Clinics, last update: 8 June 2000. Arthro - Ophthalmopathy, Arthroophthalmopathy, Hereditary Progressive Arthroophthalmopathy Stickler syndrome is a connective tissue disorder which can include ocular findings of myopia, cataract, and retinal detachment; hearing loss which is both conductive and sensorineural; midfacial underdevelopment and cleft palate (either alone or as part of the Robin sequence); and mild spondyloepiphyseal dysplasia and/or precocious arthritis. Variable phenotypic expression of Stickler syndrome occurs both within families and between families. Interfamilial variability is in part explained by locus and allelic heterogeneity. The diagnosis of Stickler syndrome is clinically based. At present, no consensus minimal clinical diagnostic criteria exist. Mutations affecting one of three different genes (

24. Syndromes Which Often Result In Combined Vision And Hearing Loss
Stickler Syndrome. Stickler syndrome is a genetic disorder inherited as a dominanttrait. sticklers syndrome often has hip dislocations associated with it.
http://www.deafblind.com/kmoss.html
Syndromes Which Often Result in Combined Vision and Hearing Loss
by Kate Moss, Family Training Specialist, TSBVI Outreach.
Usher Syndrome is one disorder that comes to mind readily for professionals in both the field of vision and hearing when they think of syndromes which result in dual sensory impairment or deaf-blindness. However, there are many syndromes that have both vision and hearing impairment as part of the conditions that define the syndrome. It is important to be aware of these conditions, since one of the sensory disabilities is often times more evident than the other. This situation makes it easy to overlook the impact of the combined vision and hearing loss. Below some of the more common syndromes, which can manifest with both vision and hearing loss, are described. If you are interested in obtaining more detailed information about any of these conditions, you may contact:
  • National Organization for Rare Disorders P.O. Box 8923 New Fairfield, CT 06812-1783
Most of the information about these syndromes comes from reports provided by NORD. The exception is the information on Congenital Rubella Syndrome which comes from a booklet, "Congenital Rubella Syndrome: Health Care Challenges" written by Dr. Steven Parker from Boston University School of Medicine in collaboration with Perkins School for the Blind, Helen Keller National Center and St. Luke's-Roosevelt Hospital. This publication is available through Perkins School for the Blind.

25. Tidsskriftet - Artikkel
2. Bennet J, McMurray SW. sticklers syndrome. Hearing loss in the non ocular Sticklersyndrome caused by a COL11A2 mutation. Laryngoscope 2000; 110 457 61.
http://www.tidsskriftet.no/pls/lts/PA_LT.VisSeksjon?vp_SEKS_ID=441382

26. Resources | Craniofacial Center | Children's Hospital & Regional Medical Center
sticklers syndrome. Sticklers Web Site Provides medical information, networkingsupport, news and updates for families affected by sticklers syndrome.
http://www.seattlechildrens.org/our_services/clinical_services/craniofacial_cent
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This information is for educational purposes only. Your health care provider can best advise you as to the best treatment for your particular condition. Featured resource: Critical Elements of Care for Cleft Lip and Palate (PDF). Sponsored by The Center for Children with Special Needs
General Craniofacial Links
American Cleft Palate-Craniofacial Association Homepage
An international, non-profit association of health care professionals involved in treating children with craniofacial differences. Bandaides and Blackboards
A web site addressing issues of students with medical problems. Includes information for children, teens, and adults who work with them.

27. Re Wagner Sticklers Syndrome
Re Wagner sticklers syndrome. In Reply to Wagner sticklers syndrome posted by Roseon August 06, 192002 at 191756 can you die from wagners.? Follow Ups
http://www.neec.com/messages/4523.html

28. Genetic Links
PAGER info on gastroesophageal reflux, sticklers syndrome, GeneticSyndrome Support Groups online. Human Genome Project Information,
http://www.nt.net/~a815/links.htm
Related Genetic Links
CHROMOSOME SPECIFIC:
(HUGO sites offer links to related chromosome support groups) HUGO Chromosome 1 HUGO Chromosome 2 Hugo Chromosome 3 Chromosome 3 Deletion Registry ... 11Q Europe WAGR Syndrome/Aniridia network
"Reaching Out" newsletter
c/o Annie Prusakiewicz
2063 Regina
Lincoln Park, MI 48146
Email: TheMooZoo@aol.com HUGO Chromosome 12 HUGO Chromosome 13 Support organization for Trisomy 13, 18 and Related Disorders ... Sanger Center. Studying Chromosome 22 HUGO Chromosome X HUGO Chromosome Y MISCELLANEOUS GENETIC LINKS Canadian Directory of Genetic Support Groups Chromosome Help Station Rainbow Families, a site that offers a great e-mail list for families who have children with trisomies Chromosome Deletion Outreach ... Genetic Alliance Helps new groups form, and directs you to appropriate support groups National Organization for Rare Disorders Useful, searchable database of rare disorders. Also offers parent matching registry

29. Disabled Writers Group
Hi my name is Danielle I m 19 years old with sticklers syndrome and RhuematoidArtritis. Dear Danielle,. I too have sticklers syndrome.
http://groups.msn.com/DisabledWritersGroup/tellyourstory.msnw?action=get_message

30. Resources - Guidance Inventory (District Office)
Disorders; Speech/Language Disorders; sticklers syndrome; TourettesSyndrome; Williams Syndrome. DIVORCE (Mary s Office). The Boys Girls
http://www.k12.nf.ca/vista/resources/inventory/d.html
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Books:
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31. Pierre Robin Network Message Central: Re: Cleft Palate Related Syndrome
I have done some research and think it could be sticklers syndrome. Ihave done some research and think it could be sticklers syndrome.
http://members3.boardhost.com/PierreRobinNet/msg/2804.html
Pierre Robin Network Message Central
Post a Response
Pierre Robin Network Message Central
    Re: Cleft Palate related syndrome Posted by Sara Arms on 3/23/2004, 1:50 pm , in reply to " Cleft Palate related syndrome
    Hi! I find it interesting that your son has webbed toes. They also run in my family but it is due to a syndrome known as Waardenburg syndrome. It most often causes two different colored eyes, premature greying or grey stripes in the hair and in its most aggressive form, complete deafness. My son Caleb is 16 months old and was born with a cleft palate and a very mild form of PRS. In the beginning our genetic specialist was concerned that Caleb may have been affected by Waardenburg as in very rare cases it can cause clefting but he does not have the web toes like I do nor does he show any other definite signs at this point. Now they are leaning more towards Stickler as he does have a slight dip in his chest known as Pectis excavatum. Please let me know if I can be of any help. Good luck! Sara Previous Message
    : I have a son that is 15 years old. He has a

32. Stickler's Syndrome In Health > Support Groups > Conditions And Diseases
Dave Hawley s Stickler Syndrome Page. Indexes online information relatedto Stickler s Syndrome. Metasearch the web for sticklers syndrome
http://ilectric.com/glance/Health/Support_Groups/Conditions_and_Diseases/Facial_
Home Metasearch Browse News ... Login/Out
Choose a Search Metasearch - The Web Metasearch - This Site Metasearch - News Metasearch - Forums Metasearch - MP3s Metasearch - Code Metasearch - Shopping Directory - Within This Category Only Directory - Entire Category - Arts Category - Business Category - Computers Category - Games Category - Health Category - Home Category - News Category - Recreation Category - Reference Category - Regional Category - Science Category - Shopping Category - Society Category - Sports Category - World Shopping - All products Shopping - Books Shopping - Electronics Shopping - Popular music Shopping - Classical music Shopping - DVD's Shopping - VHS Videos Shopping - In Theaters Shopping - Toys Shopping - Computer Hardware Shopping - Software Shopping - Magazines Shopping - Photo Shopping - Garden / Outdoor Living Shopping - Baby Shopping - Kitchen Lookup - Domain in Whois Lookup - Domain Availability Lookup - HTTP Source Lookup - DNS Record
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Practical Genetic Counselling
- by Peter S. Harper
Your Cleft-Affected Child: The Complete Book of Information, Resources, and Hope

33. University Of Dundee: Press Office Media Guide 2002 Directory Of Experts (News)
Expertise Cleft Lip and Palate craniofacial anomalies such as Treacher CollinsSyndrome, Van der Woude Syndrome, sticklers syndrome, Binders Syndrome and
http://www.dundee.ac.uk/pressoffice/mediaguide02/staff/staffm/petermossey.htm
Professor Peter Mossey
Department/School: Unit of Dental and Oral Health Expertise: Cleft Lip and Palate: craniofacial anomalies such as Treacher Collins Syndrome, Van der Woude Syndrome, Sticklers Syndrome, Binders Syndrome and Pierre Robin anomaly.
Gene/environment interaction in birth defects, smoking and birth defects
Orthodontics: with particular interest in craniofacial growth and development and genetics of dental anomalies such as hypodontia, and of the hereditary influences on development of malocclusion.
Tristan da Cunha: the Dental School provides dental care for the inhabitants of the remote island of Tristan da Cunha. The high prevalence of certain diseases on the island such as asthma has led to genetic investigations. Work: Home: Mobile: Email: p.a.mossey@dundee.ac.uk Department profile: http://www.dundee.ac.uk/dentalschool/ University Home Page Press Office Home Page Media Guide Home ... Email
University of Dundee, Press Office, Dundee, DD1 4HN

34. Stickler Syndrome
Table of Contents. Message Board. A place to call home, where you are never alone. Stickler syndrome. In 1965, Dr. Gunnar B. 1980's, this condition has been called Stickler syndrome. sticklers is
http://www.pierrerobin.org/sticklersyndrome.html
Home New parents About Us Support ... Message Board A place to call home, where you are never alone Stickler Syndrome In 1965, Dr. Gunnar B. Stickler published a five year study entitled "Hereditary Progressive Arthro-Ophthalmology," associating severe ocular degeneration with degenerative joint changes. Since the 1980's, this condition has been called Stickler Syndrome. Sticklers is a genetic (in approximately 75% of the cases) connective tissue disorder which can affect the joints, eyes, palate, heart and hearing. It is an autosomal dominant trait, meaning that it can be passed on to both boys and girls from either parent. It only requires one parent to be affected. With each pregnancy, there is a 50% chance that the child will inherit Stickler Syndrome. Sticklers is an under diagnosed disorder because a patient can be affected in only certain areas. It is possible for other family members to affected differently and even more or less severely. Families are frequently not aware that they have Stickler Syndrome until a child is born with a palate abnormality, has early degenerative joint changes or a retinal detachment. If a child with PRS doesn't present with symptoms of Sticklers in infancy, they still could show up as the child gets older. Genetic testing is available but is found to be quite expensive and not perfected yet. Continued vigilance in vision, hearing and scoliosis screening needs to be maintained during childhood.

35. Dictionary Definition Of STICKLER'S SYNDROME
Dictionary definition of STICKLER S syndrome. Medical dictionary. Synonym Stickler ssyndrome. Please select first two letters of word you are looking for.
http://www.dictionarybarn.com/STICKLERS-SYNDROME.php
Dictionary definition of STICKLER'S SYNDROME
Browse Dictionary by alphabet A B C D ... Z Top Words ST junction
St. Louis encephalitis virus

St1C1 N-hydroxyarylamine sulfotransferase

stab
...
standard pressure

Autosomal dominant arthro-ophthalmopathy associated with progressive multiple dysplasia of the epiphyses, overtubulation of long bones, cleft lip and palate, hypermobility of joints, flattened vertebral bodies, pelvic bone deformities, and deafness.
Synonym: Stickler's syndrome.
Please select first two letters of word you are looking for SA SB SC SD ... SZ fiSearchFormMaxSetId='AX006027'; Top Words standard score
standard solution

standard state

standard substance
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36. AllRefer Health Health Links Directory Support Groups
Support Groups Conditions and Diseases Facial Differences Stickler sSyndrome . Uncover resources and links to Web sites related
http://health.allrefer.com/links/facial-differences-sticklers-syndrome.html

37. EUROCRAN: Stickler Syndrome
Stickler syndrome sticklers www.sticklers resources and references.The Stickler syndrome Support Group (SSSG) www.stickler.org.uk.
http://www.eurocran.org/content.asp?contentID=1319

38. Website Of Björn Stickler
Dave Hawley s Stickler syndrome Page. Dave Hawley s Stickler syndrome Page. ..sticklers.org/ or the Stickler syndrome Support Group (UK) website at
http://collector.intex.ath.cx/stickler.html
Website of Bj¶rn Stickler Home Software Information Links ... Contact
News
update for the winamp 5 plugin which fixes the bug with ir-codes received twice new version of the winamp 5 plugin with support to display info on a 4x20 LCD created a page for IO-Warrior software Winamp 5 plugin for IR remote control with the IO-Warrior available added TimeDataPlot, a free asp.net control to downloads updated GPX verion (1.53) with some bugs fixed added more E00 vector map downloads on GPX page website is back up - using iis 6 as webserver added eSec secure data storage to downloads server harddisk crash - lost some data - page down for maintenance removed apache server in front of tomcat complete new xhtml conform pages and layout show all news
visitors since 17.09.2000 Statistics Imprint Bj¶rn Stickler

39. What We Know About Sticklers
WHAT WE DO KNOW ABOUT STICKLER syndrome. Stickler syndrome. Synonyms.arthroophthalmopathia hereditaria. arthro-ophthalmopathy (AO, AOM).
http://hometown.aol.com/coach001/page2.html
Main Other Support htmlAdWH('7002568', '234', '60'); WHAT WE DO KNOW ABOUT STICKLER SYNDROME Stickler Syndrome Synonyms
arthro-ophthalmopathia hereditaria arthro-ophthalmopathy (AO, AOM) hereditary arthro-ophthalmopathy hereditary progressive arthro-ophthalmopathy
Summary
Progressive myopia beginning in late childhood, vitreoretinal degeneration, retinal detachment causing blindness, cataracts, hearing loss, cleft palate, and spondyloepiphyseal dysplasia.
The craniofacial features range from essentially normal face to dish facies with micrognathia, depressed bridge of the nose, long philtrum, and prominent eyes. Patients with Stickler syndrome often have the feature of Robin syndrome (brachygnathia, cleft palate, glossoptosis, and backward and upward displacement of the larynx). Some cases have mental retardation.
The clinical manifestations are variable and may differ from one patient to another.
Stickler syndrome shares many characteristics with the Marshall, Wagner, and Walden syndromes and is sometimes designated as the Marshall-Stickler, Wagner-Stickler, or Walden syndrome. The radiographic characteristics of the

40. Cleft Advocate - Syndromes
Retrognathia. SaethreChotzen. Shprintzen syndrome (See VeloCardioFacialsyndrome). Stickler syndrome. sticklers.org. Definition, information
http://www.cleftadvocate.org/syndromes.html
@import url(http://www.homestead.com/~media/elements/Text/font_styles.css); Amniotic Band Syndrome
Amniotic Band Syndrome

Information and personal stories
ABS Support Network

A Yahoo group
The ClubFoot Club

About ABS and its many manifestations, including cleft lip and palate
Apert Syndrome
A Guide to Understanding Apert Syndrome

From the Children's Craniofacial Association
Aperts Overview
Discusses similarities between Aperts and Crouzons Teeter's Page www.apert.org The Apert Listserv Correspond with other Aperts families Arhinia Simply Kristi An incredible website! Beckwith-Wiedemann Beckwith-Wiedemann Syndrome From the Pediatric Database (refers to midface hypoplasia) The Beckwith-Wiedemann Support Group Information and support includes on-line support group Beckwith-Wiedemann Group UK Birthmarks/Hemangiomas/Vascular Malformations Birthmarks.com Frequently asked questions, treatment resources and more My Port Wine Stain Personal stories and links to information on treatment, make-up and more! Skin Tumors, Vascular Lesions, Face and Neck Co-authored by Jeffrey S Zapalac, MD and John E McClay, MD Hemangioma News Line Information and newsletter Hemangiomas of the Head and Neck By Bert W. O'Malley, MD

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