21. Prader Willi Syndrome Q&A praderwilli syndrome is one of the 10 most common conditions seen in genetics Early diagnosis of prader-willi syndrome gives parents an opportunity to http://www.thearc.org/faqs/pwsynd.html

Prader-Willi Syndrome by Prader-Willi Syndrome Association (USA What is Prader-Willi syndrome (PWS)? PWS is a complex genetic disorder that includes short stature, mental retardation or learning disabilities, incomplete sexual development, characteristic behavior problems, low muscle tone, and an involuntary urge to eat constantly, which, coupled with a reduced need for calories, leads to obesity. Does PWS run in families? Although PWS is associated with an abnormality of chromosome 15, it is generally considered not to be an inherited condition, but rather a spontaneous genetic birth defect that occurs at or near the time of conception. PWS is found in people of both sexes and all races. How common is this problem? About 1 in 14,000 people in the U.S. are estimated to have PWS, and the birth rate may be even higher. Prader-Willi syndrome is one of the 10 most common conditions seen in genetics clinics and is the most common genetic cause of obesity that has been identified. Does the eating problem associated with PWS begin at birth? No, newborns with PWS are typically described as "floppy" and are unable to suck well enough to get sufficient nutrients due to the low muscle tone (hypotonia). Often they must be fed through a tube for several months after birth, until muscle control improves. Sometime in the following years, usually by preschool age, children with PWS develop an increased interest in food and quickly gain excessive weight if calories are not restricted.

22. Http//www.pwsa.co.uk/ http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. GeneReviews: Prader-Willi Syndrome Your browser does not support HTML frames so you must view praderwilli syndrome in a slightly less readable form. Please follow this link to do so. http://www.geneclinics.org/profiles/pws/

Your browser does not support HTML frames so you must view Prader-Willi Syndrome in a slightly less readable form. Please follow this link to do so.

24. Florida Department Of Children & Families Information and links for those with mental retardation, autism, cerebral palsy, spina bifida, and praderwilli syndrome. http://www5.myflorida.com/cf_web/myflorida2/healthhuman/ddp/

directory contact us newsletters first time user Programs Abuse Hotline Adoption Foster Care Adult Services ... Mental Health Health Agencies Elder Affairs Health Health Care Veterans' Affairs The Developmental Disabilities site has moved ! The new location is : http://www.dcf.state.fl.us/apd/ Please update your bookmarks to this new location. Thank you. Privacy Statement

25. Prader-Willi Syndrome Arizona Association praderwilli syndrome Arizona Association, with photos, personal stories, parenting advice, pictures, and information about PWS. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

26. Center For The Study Of Autism praderwilli syndrome is a disorder which is sometimes associated with, Some of the behaviors which are common to both prader-willi syndrome and autism http://www.autism.org/prader.html

Prader-Willi Syndrome Written by Stephen M. Edelson, Ph.D. Center for the Study of Autism, Salem, Oregon Prader-Willi Syndrome is a disorder which is sometimes associated with, but not a subtype of, autism. The classical features of this disorder include an obsession with food which is often associated with impulsive eating, compact body build, underdeveloped sexual characteristics, and poor muscle tone. Because of their obsession with food, many people afflicted with Prader-Willi Syndrome are overweight. Most individuals afflicted with Prader-Willi Syndrome have mild mental retardation. Some of the behaviors which are common to both Prader-Willi Syndrome and autism are: delays in language and motor development, learning disabilities, feeding problems in infancy, sleep disturbances, skin picking, temper tantrums, and a high pain threshold. Prader-Willi Syndrome affects approximately 1 in 10,000 people. Most individuals suffering from this disorder are missing a small portion of chromosome 15 which appears to come from the paternal side of the family. When a small portion of chromosome 15 is missing and comes from the maternal side, the person may suffer from Angelman Syndrome. The most effective form of treatment for people suffering from Prader-Willi Syndrome is behavior modification. In general, medications do not appear to very effective for these individuals.

27. WCDD Home Page Statewide advocacy organization that represents people with autism, brain injury, cerebral palsy, epilepsy, mental retardation, and praderwilli syndrome. http://www.wcdd.org/

Skip navigation Mission and Population Served Guiding Principles Background and Responsibilities ... Aging and DD (DAWN) Grassroots Advocacy Network Direct Service Workforce Employment Health ... Self Advocacy (People First WI) Waiting Lists Legislative Platforms Introduction Medicaid Program ... Search Welcome The Wisconsin Council on Developmental Disabilities was established to advocate on behalf of individuals with developmental disabilities, foster welcoming and inclusive communities, and improve the disability service system. The Council's mission is to help people with developmental disabilities become independent, productive, and included in all facets of community life. In the News: Every five years the DD Council develops a State Plan to improve the quality of life for people with developmental disabilities in Wisconsin. The Council wants your help to develop the next Plan. The Council will host in La Crosse, Ashland, Fond du Lac, Milwaukee, and Stevens Point. These are designed to get your thoughts on what you think are the best things the Council can do to help people with DD have more control over their lives and be more involved in the community. [ More details.

28. Center For The Study Of Autism Hyperlexia See Links Page. LandauKleffner Syndrome. Pervasive Developmental Disorder (PDD) prader-willi syndrome. Rett Syndrome. Williams http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

29. Ipwso.org -- International Prader-Willi Syndrome Organization International praderwilli syndrome Organisation. President s Corner July 2005. IPWSO Song Ich Auch (Me Too). Newletter Summer 2005. http://www.ipwso.org/

International Prader-Willi Syndrome Organisation President's Corner July 2005 IPWSO Song "Ich Auch" (Me Too) Newletter Summer 2005

30. Oconomowoc Developmental Training Center School, residential treatment, group homes for children developmentally disabled, emotionally disturbed with mental retardation, praderwilli syndrome, autism, dual diagnosis and others. http://www.odtc-wi.com/

Be kept up to date on what's new at ODTC and see how we're leading the way in compassionate care. E-Mail Address Name E-Mail Preference HTML Text Only Not Sure Home Employment Media Room FAQ ... Related Links At first glance, you may think you are looking at a prestigious college campus, but take a look behind the smiling faces, scenic setting and laughter and you will find the campus of a national leader in the treatment and education of children and young adults with dually diagnosed developmental disabilities and emotional disturbances. Take some time to explore what makes ODTC different from all the others. ODTC is proud to be an employee-owned company. As an employee-owned company, ODTC offers the very best in professional, compassionate care because our caregivers are also our owners! We're very proud of our dedicated and professional staff. It is through their passion and hard work that makes ODTC a special place to be. LISA ENGEN

31. Prader-Willi Syndrome Association Of Ohio Growing To New Heights praderwilli syndrome Association of Ohio Growing to new heights http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

32. Ipwso.org -- International Prader-Willi Syndrome Organization Welcome to the International Prader Willi Syndrome Organization (IPWSO) web site. Our Global Family of parents, friends, and professionals has formed a http://www.ipwso.org/home.html

Welcome Welcome to the International Prader Willi Syndrome Organization (IPWSO) web site. Our Global Family of parents, friends, and professionals has formed a dedicated partnership worldwide. We are committed to enhancing the quality of life for people with PWS and their families, giving our special children the best possible opportunities for living their lives to the fullest. Currently, our international organization has 54 member and associate member countries, representing some 25,000 families. Being a member provides many advantages such as the opportunity to be a part of a worldwide network of information involving professionals, and families. Regional and international conferences are especially helpful in giving families the occasion to meet other families with similar challenges and to come together for educational workshops and lectures. Professionals are given opportunities for a universal exchange of research, experiences, and ideas. IPWSO is an organization without bordersopen to people of all origins and cultures. Please check our website and see if your country has a national association. If not, contact us and we will assist you in forming an organization and will connect you to other resources in your region, as well as throughout the world. We welcome you to join our global family! Welcome IPWSO President Contact Webmaster Hosted by: 313 Group, LLC

33. Connecticut Children's Medical Center - Child Development Center Comprised of a team of specialists who provide evaluation and consultation services for children and adolescents by bridging medical, developmental, behavioral and educational facets to produce a holistic view of the child. Developmental and behavioral challenges include Asperger's, fetal alcohol syndrome, motor skills disorders, traumatic brain injury, Williams Syndrome, austism, praderwilli syndrome and Tourette's, among others. http://www.ccmckids.org/services/cdc.asp

Services Programs Site Search Overview Staff Evaluation Consultation/Training Services ... Social Skills Office Location Location: Hartford Square West Mailing Address: 282 Washington Street Hartford, CT 06106 Telephone: 860.545.8680 Fax: 860.545.9356 Contact Person Daniel Affrunti, Ph.D., Manager E-mail daffrun@ccmckids.org The Child Development Center is comprised of a team of specialists who provide evaluation and consultation services for children and adolescents by bridging medical, developmental, behavioral and educational facets to produce a comprehensive view of the child. The mission of the Child Development Center is to assist in the facilitation of an improved quality of life for children and parents who face the challenges associated with a wide range of developmental and behavioral difficulties. We believe that children can realize their potential more fully, given the appropriate diagnosis and intervention. We provide services that are tailored to the needs of the individual child, family, and referral agency. Our evaluation services range from evaluations that are highly focused and specific to those that are comprehensive and integrated. Through diagnostic evaluation and concrete recommendations, we are able to help children and their families who may be challenged by many difficulties, including: Pervasive Developmental Disorders

34. Ontario Prader-Willi Syndrome Association The Ontario praderwilli syndrome Association (OPWSA) is a non-profit, charity which was established in 1982. Our mission is to enhance the quality of life http://members.allstream.net/~opwsa/

What is Prader-Willi Syndrome? Health News Events Real Life Stories ... Wristbands Home ~NEW~ Help support PWS and increase awareness... WRISTBANDS are now available! Click here for more info and order yours today! Welcome! The Ontario Prader-Willi Syndrome Association (OPWSA) is a non-profit, charity which was established in 1982. Our mission is to enhance the quality of life for individuals with Prader-Willi Syndrome. OPWSA has a membership of 1000, including individuals with PWS, their families and interested professionals. This website was created to be a source of information for those interested in and affected by Prader-Willi Syndrome. Here you will find: - Specific information on identifying the syndrome - Updated medical research and studies - Discover the true face behind PWS - The OPWSA publishes a newsletter quarterly ... - Annual Prader-Willi Syndrome Conference The Ontario Prader-Willi Association is a registered non-profit charity organization, established in 1982. CHARITABLE NO.:

35. OPWSA: What Is Prader-Willi Syndrome? praderwilli syndrome (PWS) is a genetic condition which is generally caused by a As prader-willi syndrome becomes more widely recognized more and more http://members.allstream.net/~opwsa/whatispws.htm

What is Prader-Willi Syndrome? Health News Events Real Life Stories Newsletter ... Home What is Prader-Willi Syndrome? Prader-Willi Syndrome (PWS) is a genetic condition which is generally caused by a deletion in Chromosome 15. The current incidence of PWS is 1-12,000. It is believed that there is a close connection between PWS and disturbance of the hypothalamus-an area of the brain which controls a number of bodily systems.The following is an overview of characteristics common to Prader-Willi Syndrome. However, not all symptoms are present in all individuals and the intensity of characteristics varies from person to person: INFANTS Characteristics: Hypotonia (weak muscle tone) Difficulty with feeding because of poor sucking ability Respiratory difficulties Helpful Interventions: Most infants will benefit greatly from early interventions with a physio/occupational therapist who can help set up a program to encourage development and provide assistive devices which will help. A nutritionist can provide information about diet, ensuring that adequate calories are provided. As your baby grows, speech therapy may also enhance your child's skills. Most infants with PWS have a happy disposition and respond well to people. A pediatric endocrinologist can provide information on growth hormone therapy which can assist greatly in muscle development and growth.

36. Ontario Prader-Willi Syndrome Association OPWSA provides support and information to all those interested in finding out about this syndrome. A special emphasis on Canadian content. http://members.attcanada.ca/~opwsa/

37. Prader-Willi Syndrome / Family Village praderwilli syndrome Association (USA) is dedicated to serving individuals Positively Prader Willi Syndrome was started to provide mothers of infants http://www.familyvillage.wisc.edu/lib_pws.htm

Prader-Willi Syndrome Who to Contact Where to Go to Chat with Others Learn More About It Web Sites ... Search Google for "Prader-Willi Syndrome" Who to Contact The Prader-Willi Syndrome Association (USA) 5700 Midnight Pass Rd. Sarasota, Fla 34242 Toll-Free: (800) 926-4797 Tel: (941) 312-0400 Fax: (941) 312-0142 E-mail: Reception@pwsausa.org Web: http://www.pwsausa.org/ Prader-Willi Syndrome Association (USA) is dedicated to serving individuals affected by Prader-Willi Syndrome (PWS), their families, and interested professionals. To provide information, education, and support services to its members, PWSA offers: a toll-free telephone number for information and referrals a bimonthly newsletter, The Gathered View publications and audiovisual presentations about PWS (See Publications Available From P.W.S.A.) an annual national conference for families and professionals (See Annual PWSA(USA) National Conference) a nationwide network of local chapters, parents, and professionals See PWSA (USA) Chapters and Affiliated Organizations research funding to expand knowledge and treatment options Representation on the international level Organized in 1975 to provide a resource for education and information about Prader-Willi syndrome and support for families, professionals and other interested citizens, PWSA(USA) was first headquartered in the Minneapolis/St. Paul area, then in St. Louis, Missouri, and currently in Sarasota, Florida since October of 1997. The association is governed by a 12 member Board of Directors who, together with an executive director and four officers, are responsible for directing the organization's operations and serving the 27 state and regional chapters and their members. In addition, 11 health service professionals serve on a Scientific Advisory Board to review research proposals.

38. Suite101.com A forum to provide a support base for PWS without having to join one of the national or international associations, and to make people more aware of PWS. http://www.suite101.com/welcome.cfm/prader_willi_syndrome

Topics Articles Links Free Courses Home Directory 22 Communities What's New ... Free e-Courses Search Suite101.com Member Central Join Our Community! Login SuiteMail What's New ... Become a Feature Writer Fun Suite Full Listing Contests Scribbles SuiteCards Free Newsletters Subscribe Here! Member Update Discussion Rooms The Forum The Lounge SuiteChat The Writers' Suite Community Stores The Co-op Store Biz Center Best of Suite eBooks Book Circle Community Channels Arts and Crafts Business and Economics Computers and Technology Education ... Youth Corner New Topics California Wine Macintosh Musings Papal History My Midlife Mania ... More... New Articles Chocolate Pie and Other Easy to Make Goodies Pan-fried Fish Margaret L. Carter, Child of Twilight Towns on the Plains: An Introduction, part 2 ... More... New Discussions contact...kind of... Is It Worth It? The Price of Being Right Shall We Fiddle While Social Security Burns? Eventually, you find them boring ... More... Suite Events Memories of Grandparents Post-Soviet Nations Fall Food Festival Suite University Visit the University About Suite University Suite University News Course Listing ... Student Testimonials New Free Courses Introduction to Hinduism The Last Charge: Culloden and the 'Forty-five Writing: A How-To for Kids Dreams and the Subconscious Mind ... More...

39. Prader-Willi Syndrome Genes and disease provides short descriptions of inherited disorders. It is hosted by the National Center for Biotechnology Information (NCBI), http://www.ncbi.nlm.nih.gov/disease/prader.html

This Genes and Disease page has been moved to: Please update your bookmarks. If you are not automatically transported to the new page after 15 seconds, click on this link Genome View SNRPN on chromosome 15 Databases PubMed the literature LocusLink collection of gene-related information OMIM catalog of human genes and disorders Information Prader-Willi Syndrome Association (USA) information, education, and support services GeneClinics a medical genetics resource PRADER-WILLI SYNDROME (PWS) is an uncommon inherited disorder characterized by mental retardation, decreased muscle tone, short stature, emotional lability and an insatiable appetite which can lead to life-threatening obesity. The syndrome was first described in 1956 by Drs. Prader, Labhart, and Willi. PWS is caused by the absence of segment 11-13 on the long arm of the paternally derived chromosome 15. In 70-80% of PWS cases, the region is missing due to a deletion. Certain genes in this region are normally suppressed on the maternal chromosome, so, for normal development to occur, they must be expressed on the paternal chromosome. When these paternally derived genes are absent or disrupted, the PWS phenotype results. When this same segment is missing from the maternally derived chromosome 15, a completely different disease, Angelman syndrome , arises. This pattern of inheritance - when expression of a gene depends on whether it is inherited from the mother or the father - is called genomic imprinting. The mechanism of imprinting is uncertain, but, it may involve DNA methylation.

40. OMIM - PRADER-WILLI SYNDROME; PWS http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176270

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