41. Smith-Magenis Syndrome : Genetic Disorders : Disorders And Diseases : Health And PRISMS (Parents and Researchers Interested in smithmagenis syndrome) http//www.smithmagenis.org. Details about the international support group http://www.internet-web-directory.com/Health_and_Fitness/Disorders_and_Diseases/

Skip to Content Login/Register Web Directory by Internet-Web-Directory.com Web Directory Home ... Link Notify Search the entire directory only this category Advanced Search Web Directory Health and Fitness Disorders and Diseases ... Genetic Disorders Smith-Magenis Syndrome Smith-Magenis Syndrome Subscribe Links PRISMS (Parents and Researchers Interested in Smith-Magenis Syndrome) http://www.smithmagenis.org Details about the international support group organization and its mission as well as the condition. Includes an introduction, diagnosis, parent's corner, meet other people with SMS and educational considerations. More Details Review It Rate It Bookmark It Sponsor Links Love Romance Dating Gift Ideas at Gifts-Shop.com Internet-Web-Directory.com

42. Autism Support Group - What Is Smith-Magenis Syndrome ? What is smithmagenis syndrome? A syndrome is a recognizable pattern of smith-magenis syndrome (SMS) is associated with a small, missing section (called http://momofautistic.proboards30.com/index.cgi?board=Labels&action=display&threa

43. Server/Human/doc : Abstract smithmagenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome associated with behavioral abnormalities and sleep http://veille-srv.inist.fr/bin/dilib/AppliHuman2/doc.fibres.cgi?/applis/veille/h

44. Smith-Magenis Syndrome - H Texas Online Family’s plight promotes awareness about smithmagenis syndrome through a blood test, diagnosed Sarah with smith-magenis syndrome (SMS). http://www.htexas.com/feature.cfm?Story=338

45. Smith-Magenis Syndrome About smithmagenis syndrome - report from the 1st national Conference on the smith-magenis syndrome. smith-magenis syndrome NORD - smith-magenis syndrome http://www.ability.org.uk/Smith_Magenis_Syndrome.html

"see the ability, not the disability" You to can help support the Ability Project by: Our Aims ... Z Smith-Magenis Syndrome About Smith-Magenis Syndrome - report from the 1st national Conference on the Smith-Magenis Syndrome. Smith-Magenis syndrome NORD - Smith-Magenis Syndrome Contact Group Smith Magenis Syndrome (SMS) Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

46. SSBP - Society For The Study Of Behavioural Phenotypes Nearly all cases of smithmagenis syndrome occur de novo (Zori et al., 1993). Individuals with Smith Magenis syndrome are reported to have http://www.ssbp.co.uk/files/syndromes/smithmag.htm

SSBP Information Sheet SMITH MAGENIS SYNDROME First description: Incidence/prevalence It is believed that there are many unreported cases of Smith-Magenis syndrome. As a result, Greenberg et al. (1991) suggest that the literature is misleading in terms of its reported incidence. Greenberg et al. propose a minimum birth prevalence of one in 1 in 25,000 births and suggests that SMS may be as common as Prader-Willi syndrome (1 in 16,000, Burd et al., 1990). Genetic aspects: Nearly all cases of Smith-Magenis syndrome occur de novo (Zori et al., 1993). SMS is a microdeletion syndrome associated with an interstitial deletion of the short arm of chromosome 17, specifically band 17(p11.2p11.2)(Smith et al., 1986). Recent research has suggested that SMS is caused by a mutation in a single candidate gene, RAI1 (Slager et al., 2003). Physical phenotype: Cognitive characteristics: Although the level of intellectual disability in SMS is variable, the majority of individuals are reported to fall in the moderate range of cognitive impairment, with varied adaptive skills. The severity of the learning disability correlates with the size of the 17p11 deletion. Additionally, speech and language development is markedly delayed, particularly in relation to expressive language (Greenberg et al., 1991, 1996). Children and adults with SMS have been described as displaying a good memory together with good perceptual skills and excellent computer skills.

47. Www.ddhealthinfo.org - Medical Care Information smithmagenis syndrome is a distinct and clinically recognizable contiguous smith-magenis syndrome (SMS) is caused by a de novo genetic change early in http://www.ddhealthinfo.org/ggrc/doc2.asp?ParentID=5196

48. Smith-Magenis Syndrome, Eastern Carolina smithmagenis syndrome - University Health Systems of Eastern Carolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county, outebanks counties in http://www.uhseast.com/117786.cfm

Health News Health Library Health Topics Healthy Living ... Nutrition Self-Help Resources Information about national and local self-help organizations and support groups. Smith-Magenis 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. International network. Founded 1993. Parent to parent program offering support, advocacy and education for families affected by Smith Magenis syndrome. Information, referrals, literature, phone support and newsletter. Dues $30. WRITE: PRISMS P.O. Box 741914 Dallas, TX 75374-1914 CALL: 972-231-0035 E-MAIL: info@prisms.org WEBSITE: http://www.prisms.org VERIFIED: 10/20/2004 The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information. For additional information on self-help groups, please visit the American Self-Help Group Clearinghouse web site at http://www.mentalhelp.net/selfhelp

49. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Genetic_Disorders/ The CaF Directory A definition of smith-magenis syndrome, PRISMS (Parents and Researchers Interested in smith-magenis syndrome) - Details about the http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Genetic_Dis

@import "/styles/navbar.css"; @import "/styles/tabStyles.css"; Set home page Bookmark site Add search Latest News ... Email to friend Text Size A A A Front Page ... Genetic Disorders : Smith-Magenis Syndrome Subtopics See Also: Health: Conditions and Diseases: Rare Disorders Search Google: Smith-Magenis Syndrome News Books Links ... UF Scientist Finds Unexpected Link Between Cat And Human AIDS Viruses (September 9, 2005) full story Mayo Clinic Develops New Coma Measurement System (September 8, 2005) full story Nitric Oxide Could Extend Fertility (September 8, 2005) Biochemistry , an American Chemical Society journal. full story New Anti-thrombotic Therapy Effective, Safer For Patients (September 7, 2005) full story Olive Oil Contains Natural Anti-inflammatory Agent (September 6, 2005) full story Flipped, Expelled, Copied, And Shrunk: Researchers Document Dramatic Genome Alterations During Primate Evolution (September 6, 2005) Genome Research presents a series of studies that provide insight into the evolution and variation of primate genomes. The issue will appear online and in print on September 1, concomitant with the publication of the chimpanzee genome sequence in the journal Nature full story Discovery Will Aid Identification Of Misregulated Genes In Rett Syndrome (September 4, 2005)

50. Smith smithmagenis syndrome. Examinations Photographs Movies Links Home Search noJava Home. http://medgen.genetics.utah.edu/photographs/pages/smith.htm

Smith-Magenis syndrome Examinations Photographs Movies Links ... noJava Home

51. Smith Magenis Chromosome (syn. Of Smith-magenis Syndrome) ThirdAid.com the world s first dedicated online patient to patient medical help community. http://www.thirdaid.com/conditions/Smith_Magenis_Chromosome.htm

52. Smith-Magenis Syndrome NeuroLearn NeuroHelp Neurodevelopmental Summary smithmagenis syndrome is characterized by mental retardation and multiple congenital anomalies. A deletion at chromosome 17p11.2 is seen in most http://moon.ouhsc.edu/kfung/JTY1/NeuroHelp/ZNP2IE05.htm

Smith-Magenis syndrome NeuroLearn NeuroHelp Neurodevelopmental Disorders Background ... Reference BACKGROUND AND CLINICAL INFORMATION Head Summary: Smith-Magenis syndrome is characterized by mental retardation and multiple congenital anomalies. A deletion at chromosome 17p11.2 is seen in most patients by cytogenetics or, in smaller deletion, by FISH. The deletion occurs in only one chromosome and almost all of the patients have de novo deletions. Smith-Magenis syndrome is characterized by typical craniofacial features, peripheral neuropathy, mental retardation, and hyperactivity disorder or ADHD. Other typical problems include onychotillomania, spasmodic upper body squeezing, and sleep behavior. Typically, these patients also have aggression, self–destruction, and tantramus. Renal, musculoskeletal, cardiac, and ophthalmological abnormalities may also be present. Incidence: 1/25,000 in the general population. This can be an underestimation. Genetics: Deletion at chromosome 17p11.2. The deletion vary from 1.5 MB to 9 MB but they typically are about 5 MB in size. Haplotype insufficiency: Deletion occurs on only one chromosome.

53. Health/Conditions And Diseases/Genetic Disorders/Smith-Magenis Syndrome -- The D A definition of smithmagenis syndrome, its inheritance pattern, PRISMS (Parents and Researchers Interested in smith-magenis syndrome) http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Genetic_Disor

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites report abuse/spam url: report-abuse.dmoz.org/?cat=Health/Conditions_and_D... The CaF Directory A definition of Smith-Magenis syndrome, its inheritance pattern, pre-natal diagnosis and a support group in the United Kingdom. url: www.cafamily.org.uk/Direct/s33.html NORD: Smith Magenis Syndrome Offers the synonyms, a general discussion and further resources. url: www.rarediseases.org/search/rdbdetail_abstract.htm... PRISMS (Parents and Researchers Interested in Smith-Magenis Syndrome) Details about the international support group organization and its mission as well as the condition. Includes an introduction, diagnosis, parent's corner, meet other people with SMS and educational considerations. url: www.prisms.org

54. Welcome To Bridges4kids.org! Parents Researchers Interested in smithmagenis syndrome (PRISMS) For more information on smith-magenis syndrome, please see the following references http://www.bridges4kids.org/Disabilities/SMS.html

Early On Lead Poisoning Positive Behavior Support No Child Left Behind ... LDA of Michigan Where to find help for a child in Michigan Anywhere in the U.S. , or Canada What's New? Help Text Menu ... Translate Last Updated: Disability Information - Smith-M a genis Syndrome (SMS) General Information Articles Related to this Disability Medical Information back to the top ... report a bad link General Information What is Smith-Magenis Syndrome (SMS)? from http://www.specialchild.com/archives/dz-027.html Smith-Magenis syndrome (SMS) is a distinct and clinically recognizable genetic disorder characterized by a specific pattern of physical, behavioral, and developmental features. SMS, which was first described in the early 1980's by Ann C.M. Smith, MA (a genetic counselor) and Ellen Magenis, MD (a cutogeneticist), is the result of a deletion of chromosome 17 (17p11.2). The chromosomal deletion occurs from a spontaneous genetic change (mutation) that happens for unknown reasons, therefore, it is not a familial disorder. SMS is considered a rare disorder and is estimated to occur in 1 out of every 25,000 live births. Currently there are over 100 cases reported, however, it is believed that SMS is widely under diagnosed because clinical features may be subtle. It is expected that with increased awareness, the number of those identified as having SMS will increase.

55. Smith-Magenis Syndrome: Home identifiying smithmagenis syndrome and treatments in the educational setting. Though there is no known cure for smith-magenis syndrome, there are many http://www.people.virginia.edu/~mmk5r/302_website/

Welcome to our website! P icture taken from PRISMS media gallery. This website is geared towards parents and teachers looking for information concerning the characteristics used for identifiying Smith-Magenis Syndrome and treatments in the educational setting. Though there is no known cure for Smith-Magenis Syndrome, there are many intervention techniques and educational strategies that can be used to combat the characteristics asssociated with the syndrome. We hope this website offers whomever views it information about and additional resources regarding Smith-Magenis Syndrome. Overview History: first identified by Ann Smith and Ellen Magenis in the early 1980's (Haneghan, 603). Incidence rate: about 1/25,000 in general population (Hagerman, 341) and ranges from birth to 72 years of age (Cassidy and Allanson, 363). Definition: Smith-Magenis Syndrom is a chromosomal disorder characterized by a recognizable pattern of physical, behavioral, and developmental features (

56. Journal Of Pediatric Orthopaedics B - UserLogin The orthopaedic manifestations of smithmagenis syndrome smith-magenis syndrome is a rare condition, which occurs due to interstitial deletion of http://www.jpo-b.com/pt/re/jpedorthob/fulltext.01202412-200301000-00004.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive You are attempting to access protected content. To access this content please login using an established account or create/activate an account. If you have already created/ activated an online account, please login below: User Name: Password: Note: passwords are CASE SENSITIVE If you are a new user or guest visiting an LWWonline site for the first time, please complete the new account setup process to view or purchase content. Forgot your password? Subscribe Renewal Information Subscribe to RSS feed utrdc-pt02 Release 4.0

57. Genome.gov | 2nd National Conference On Smith-Magenis Syndrome Overview of the September 2000 2nd National Conference on smithmagenis syndrome and the SMS Research Roundtable. Includes an address where one can obtain http://www.genome.gov/10000238

triggerParms["cpp_5"] = "Referer:"+ cppUrlPatch (""); // Optional Home About NHGRI Newsroom Staff ... Calendar of Events 2nd National Conference on Smith-Magenis Syndrome Print Version Second National Conference on Smith-Magenis Syndrome Bridging Past and Future Horizons: Understanding the SMS Puzzle September 2000 An educational conference on Smith-Magenis Syndrome (SMS) was held on Sept 21-24, 2000 at the Key Bridge Marriott, Arlington, VA. The conference was co-sponsored by the National Human Genome Research Institute (NHGRI) and the National Institutes of Health (NIH) Office of Rare Diseases (ORD), in conjunction with the parents' support group Parents and Researchers Interested in Smith-Magenis Syndrome (PRISMS ). The conference series brought together parents, researchers and professionals caring for persons with SMS to exchange information, ideas, scientific data and family experiences. Attendees hear from medical experts, geneticists,and parents about the latest information on the medical, social, developmental and behavioral aspects of SMS, as well as current research efforts into the cause, management and effective treatment of SMS. The format of invited speakers and a series of smaller, more hands-on workshops is designed to maximize the exchange of information between parents and professionals from a variety of specialties. Additional information is available through PRISMS: 76 S. New Boston Road

58. Health Library - smithmagenis syndrome Parent to parent program offering support, advocacy and education for families affected by Smith Magenis syndrome. http://yalenewhavenhealth.org/library/healthguide/en-us/SelfHelp/topic.asp?hwid=

59. Journal Of The American Academy Of Child & Adolescent Psychiatry - UserLogin I am reporting a case of smithmagenis syndrome (SMS) diagnosed serendipitously by (1991), Molecular analysis of the smith-magenis syndrome a possible http://www.jaacap.com/pt/re/jaacap/fulltext.00004583-199811000-00010.htm

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60. Karger Publishers smithmagenis syndrome is associated with a microdeletion of the short arm of We describe a fetus in which the diagnosis of smith-magenis syndrome was http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

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