1. Turner Syndrome Society - Home Mission is to increase public awareness and understanding of turner syndrome; increase understanding of those affected by turner syndrome about the http://www.turner-syndrome-us.org/

TS Conference Join Our E-mail list Volunteers Needed Announcements News from National - 9-8-05 Invitation to Take TSSUS Survey TS Aortic Dissection Registry TS Journal Discover a Slew of TS News in Scenic Seattle Patient Age Must Be Considered When Reviewing Hormone Replacement Therapy Studies The Story of Maria See all the benefits of membership by joining the TSS today. TSS has locations all over the globe. Check out our worldwide organizations. Or, find a local chapter near you. TURNER SYNDROME SOCIETY of the United States 14450 TC Jester, Suite 260, Houston T 77014 Toll Free 800-365-9944; P: 832-249-9988; F: 832-249-9987 t ssus@turner-syndrome-us.org Join Our E-mail list Media Meets BBB guidelines for giving and AFP Member The Turner Syndrome Society of the United States is a not fo profit organization recognized as tax exempt under Internal Revenue Code section 501(c)(3).

2. NORD - National Organization For Rare Disorders, Inc. National Organization for Rare Disorders is dedicated to helping people with rare, orphan diseases. Rarediseases.org contains information on the prevention, http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Turner Syndro

3. Turner Syndrome, Its Symptoms And Treatments turner syndrome is one of the rare diseases that affect only girls. Short stature and a webbed neck are the most obvious signs of turner syndrome. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. Turner Syndrome Society - FAQ turner syndrome is a chromosomal condition that exclusively affects girls and turner syndrome is caused by the complete or partial absence of one of the http://www.turner-syndrome-us.org/resource/faq.html

What is Turner syndrome? Turner syndrome is a chromosomal condition that exclusively affects girls and women. It occurs when one of the two X chromosomes normally found in females is missing or incomplete. The syndrome is named after Dr. Henry Turner, who was among the first to describe its features in the 1930's. What causes Turner syndrome? Turner syndrome is caused by the complete or partial absence of one of the two X chromosomes normally found in women. How is Turner syndrome diagnosed? A blood test, called a karyotype, analyzes the chromosomal composition of the individual. This is the most commonly used blood test to diagnose Turner syndrome. Does any one thing cause Turner syndrome? No. Turner syndrome is not associated with any environmental or any other factors generally associated with genetic problems. Despite many efforts, no real causes have been found to be linked to this condition. It appears to be a random event that can happen to anyone. What are the most common characteristics of Turner syndrome? The most common characteristics of Turner syndrome include short stature and lack of ovarian development. A number of other physical features, such as webbed neck, arms that turn out slightly at the elbow, and a low hairline in the back of the head are sometimes seen in Turner syndrome patients. Individuals with Turner syndrome are also prone to cardiovascular problems, kidney and thyroid problems, skeletal disorders such as scoliosis (curvature of the spine) or dislocated hips, and hearing and ear disturbances.

5. Turner's Syndrome Society, Texas Providing links and information about Turner's Syndrome. Definition and Synonyms, FAQ, TSS Societies (National, State, and Local), Associated Links http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. About Turner Syndrome (Canada) The Turner s Syndrome Society of Canada, a nonprofit charitable organization, was founded in 1981 by an individual with TS who wanted to share http://www.turnersyndrome.ca/

This site is an information resource for those affected by, or interested in Turner's Syndrome. Good places to start are: "About the Society," or "Got Questions?" Challenges, opportunities and goals of our national organization today. In a recent letter from the President, these matters are discussed. Please follow the links below to read her remarks and to participate in two surveys which will help chart our course in the years ahead. A letter from the president. Educational Resources Questionnaire. Member Needs Questionnaire. The Turner's Syndrome Society's 25th Annual Conference will be held in Edmonton, Alberta in the spring of 2006. Please watch here for further details. We wish to thank the following sponsors for their generous donations to our 24th Annual Conference which was held in Ottawa, Ontario from April 15 to 17, 2005: - Eli Lilly Canada Inc. - Serono Canada Inc. The Turner's Syndrome Society of Canada, a non-profit charitable organization, was founded in 1981 by an individual with TS who wanted to share experiences and information. It provides support services for individuals with TS and their families and disseminates up-to-date medical information to families, physicians and the general public. The Society is run by individuals with TS and their families, supported by professionals and governed by a Board of Directors.

7. Justin's Home Page Hi there, thanks for visiting my home page. I have dedicated this page to my family, special my daughter who has turner syndrome, therefore you will find a lot of information About turner syndrome here at my page. http://home6.inet.tele.dk/justin/explore.htm

Justin's Home page Hi there, thanks for visiting my home page. I have dedicated this page to my family, special my daughter who has Turner Syndrome, therefore you will find a lot of information About Turner Syndrome here at my page. My name is Justin i am 26 years old and living together with my girlfriend Bettina(25 years) and our little daughter Natascha (10 months old) We live in Denmark in a town called Viborg in Jylland. I like to play with Computers, read books and watch a good movie, Bettina like to read a good book, or watch a movie. We like to walk long trips with Natascha, play with her, she loves when we crawl after her, and be lifted up over our head and down again, she likes our food, so we can never eat our dinner for ourselves, she still like too wakes up in the night, just to get a little attention, and that's not so funny anymore. Below are there some links to Turner Syndrome page, and other pages i like. Pages about Turner Syndrome The Rooyal Danish Famiy The Danish Weather, also in English Shubidua a danish rockband, there are samples to hear

8. Turner's Syndrome, Definition Schereshevkiiturner syndrome Turner-Varny Syndrome. Clinical Abnormalities and Approximate Incidence. Short Stature 100% Ovarian Failure 90% http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. About Turner Syndrome Turner s Syndrome is a condition that affects about one in every 2500 females. Unlike females without Turner s Syndrome who have two X chromosomes, http://www.turnersyndrome.ca/got_quest.html

What is Turner's Syndrome? Turner's Syndrome is a condition that affects about one in every 2,500 females. It was first described in 1938 by Dr. Henry Turner who observed a set of common physical features in some of his patients. However, it was not until 1960 that a chromosomal abnormality was found. Intellectually, girls with Turner's Syndrome are not at risk for mental retardation, but they may have learning problems, especially in arithmetic. Many also have greater difficulty on tasks requiring spatial skills, like map reading, puzzles, visual organization. Although they are not at increased risk for psychological problems, many do have decreased self-esteem and problems with body image. Children with Turner's Syndrome may also be hyperactive. Identifying Features of the Condition: Short stature (mean height of 4'7") Lack of secondary sexual characteristics and infertility Medical problems such as ear, eye, heart, kidney or thyroid difficulties, sugar diabetes, high blood pressure and keloid healing Secondary features such as low set ears, low hairline, webbed neck, pigmented moles, bending out of the elbows, and puffy hands and feet.

10. About Turner Syndrome (Canada) The Turner's Syndrome Society of Canada, a nonprofit charitable organization, was founded in 1981 by an individual with TS who wanted to share experiences and information. It provides support services for individuals with TS and their families and disseminates up-to-date medical information to families, physicians and the general public. (In French and English.) http://www.TurnerSyndrome.ca/

This site is an information resource for those affected by, or interested in Turner's Syndrome. Good places to start are: "About the Society," or "Got Questions?" Challenges, opportunities and goals of our national organization today. In a recent letter from the President, these matters are discussed. Please follow the links below to read her remarks and to participate in two surveys which will help chart our course in the years ahead. A letter from the president. Educational Resources Questionnaire. Member Needs Questionnaire. The Turner's Syndrome Society's 25th Annual Conference will be held in Edmonton, Alberta in the spring of 2006. Please watch here for further details. We wish to thank the following sponsors for their generous donations to our 24th Annual Conference which was held in Ottawa, Ontario from April 15 to 17, 2005: - Eli Lilly Canada Inc. - Serono Canada Inc. The Turner's Syndrome Society of Canada, a non-profit charitable organization, was founded in 1981 by an individual with TS who wanted to share experiences and information. It provides support services for individuals with TS and their families and disseminates up-to-date medical information to families, physicians and the general public. The Society is run by individuals with TS and their families, supported by professionals and governed by a Board of Directors.

11. Turner Syndrome Society - Home Mission is to increase public awareness and understanding of turner syndrome; increase understanding of those affected by Turner Syndrome about http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. Turner Syndrome Clinical Studies At NIH If you have any medical questions or comments about this site, send email to langei@mail.nih.gov. If you have any technical questions or comments about this http://turners.nichd.nih.gov/

If you have any medical questions or comments about this site, send email to langei@mail.nih.gov If you have any technical questions or comments about this site, send email to baileyi@mail.nih.gov Last Updated February 10, 2005

13. Turner Syndrome Society - FAQ turner syndrome Society 14450 T.C. Jester, Suite 260 Houston, TX 77014, USA. Tel 800365-9944 832-249-9988. Fax 832-249-9987 http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. Clinical Features Of Turner Syndrome http://turners.nichd.nih.gov/ClinFrIntro.html

15. About Turner Syndrome (Canada) The Turner's Syndrome Society of Canada, a nonprofit charitable organization, was founded in 1981 by an http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

16. Turner Syndrome Support Society Contains support, information on hormone replacement therapy for folks with Turner s, health issues for folks with TS, and personal stories. http://www.tss.org.uk/

Turner Syndrome Support Society Home About Us Contents Adult Care Aims ASPECTS contents Contact us Events Diary Footwear Healthcare HRT Information contents Latest News contents Living with TS Local Groups New TS Book The Society Treatment Useful Links What Is TS? Notices Annual Conference 30th Sep - 2nd Oct 2005 - Booking form now available Welcome We hope you find our website useful and friendly. The Society provides accurate and up to date information on Turner Syndrome and the many aspects of living with the condition on a daily basis. Girls and women with TS and their parents often find that what they need most is contact with others in the same situation. When you join the Society we can offer you a network for social contact with people who share the same interests and concerns. We are also happy to help health, education and other professionals and anyone who cares for someone with TS. Contact us on Tel: +44 (0)1389-380385 Fax:+44 (0)1389-380384 e-mail: Web Design by Marjen Media

17. Turner's Syndrome, Results From Genetic Disorder Tests Becoming Pregnant (How it all happens) Navigation Turner's Syndrome 45, XO Introduction Trisomy 21 - Down Syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. Turner Syndrome Support Society turner syndrome Support Society http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

19. Booklets From The Turner Center turner syndrome Treatment With Natural Estrogen by Rune Weis Naeraa et al. Transcultural study of Turner s syndrome by J. Nielsen and Marleen Stradiot http://www.aaa.dk/TURNER/ENGELSK/DOWNLOAD.HTM

Booklets from the Turner Center Turner's syndrome. An orientation Turner's syndrome: Treatment With Natural Estrogen. XYY syndrome. Klinefelter's syndrome. ... Turner´s Syndrome. An Orientation by Johannes Nielsen, Rune Næraa and Members of Turner Contact Groups in Denmark This book was written and published in Danish in 1985 on the background of a tremendous need for further information about Turner's syndrome, and a wish to extend the knowledge about Turner contact groups in Denmark. It is in no way an attempt to give a comprehensive description of all aspects of Turner's syndrome. The book has been written with the intention of providing better information for Turner girls/women, their parents and relatives, as well as for parents who have undergone prenatal examination and been informed that the cild they are expecting has Turner's syndrome. It is, however, also our hope that it will be read by genetical counsellers, doctors, teachers and others who come into professional contact with Turner girls/women and parents. There has so far been a great interest and demand for this book, and there is no doubt that it fills a gap in the available information about Turner's syndrome. Internet version for online viewing or printing.

20. The MAGIC Foundation An organization providing support and education regarding growth disorders in children and related adult disorders. Includes Growth Hormone http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 1     1-20 of 122    1  | 2  | 3  | 4  | 5  | 6  | 7  | Next 20