61. MECP2 Data Retrieval Searchable database of known and novel MECP2 disease-causing mutations and polymorphisms. From the International Rett Syndrome Association. http://mecp2.chw.edu.au/

RettBASE: IRSF MECP2 Variation Database Welcome We welcome you to the web-based IRSF Gene Variation Database (RettBASE). This database has been constructed by merging mutation and polymorphism data from the published literature pertaining to Rett syndrome and related clinical disorders, and by incorporating unpublished mutation and polymorphism data that have been submitted directly to us. RettBASE is updated on a very frequent basis manually by our curators to ensure the validity of the data being sent to us. A search engine has been constructed allowing you to perform searches of varying complexity, to obtain information relevant to your research or clinical questions. We invite you to: Browse mutation and polymorphism list for the sequence variation of your interest Perform simple or complex searches using our Boolean-based search engine Submit your unpublished sequence variation data by one of several means Alert us to published sequence variation data which we have not yet included Offer suggestions as to how we could enhance RettBASE to better meet your needs Acknowledgements Initial construction and maintenance of RettBASE could not have been possible without the very generous financial support of the International Rett Syndrome Foundation We would also like to acknowledge the New South Wales Rett Syndrome Association and the Rett Syndrome Australian Research Fund for their generous support of the NSW Rett Syndrome Research Team at the Children's Hospital at Westmead.

62. Space Coast Early Intervention Center A nationally recognized not-for-profit pre-school and therapeutic center for families and children with Down syndrome, William s syndrome, Rett syndrome, Cerebral palsy, Autism, P-4 Deletion syndrome, PDD and Apert syndrome. http://www.sceic.com/

63. Rett Syndrome -- Genes And Disease -- NCBI Bookshelf Rett syndrome (RTT) is a progressive neurodevelopmental disorder almost exclusively affecting females. With an incidence of about 1 in 10,000 births, it is a common cause of http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gnd&part=rettsyndrome

64. Rett Syndrome - Symptoms, Diagnosis, Treatment Of Rett Syndrome - NY Times Healt Free articles and multimedia from The NY Times, including information on symptoms, diagnosis, treatments, tests, and surgical procedures, as well as current news and interviews http://health.nytimes.com/health/guides/disease/rett-syndrome/overview.html

65. Rett Syndrome - Definition Of Rett Syndrome Rett Syndrome is one of the autism spectrum disorders. Rett Syndrome. By Lisa Jo Rudy, About.com Guide. Updated October 19, 2010. About.com Health's Disease and Condition http://autism.about.com/od/autismterms/g/RettDefinition.htm

zWASL=1;zGRH=1 zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zDO=0 Home Health Autism Spectrum Disorders Autism Spectrum Disorders Search Autism Spectrum Disorders Is It Autism? Life With Autism Treatments ... Share w(x2+zWl+'?p=1" zT="18/1[N" rel="nofollow">Print') Free Autism Spectrum Disorders Newsletter! Sign Up Discuss in my Forum By Lisa Jo Rudy , About.com Guide Updated October 19, 2010 About.com Health's Disease and Condition content is reviewed by the Medical Review Board See More About: autism terms autism spectrum autism basics rett syndrome zSB(3,3) Definition: Rett syndrome, a childhood neurodevelopmental disorder, is considered to be part of the autism spectrum. Unlike the other autism spectrum disorders, Rett syndrome almost always affects girls. Loss of muscle tone is usually the first symptom. Other early symptoms may include problems crawling or walking and diminished eye contact. As the syndrome progresses, girls lose purposeful use of their hands and the ability to speak. Compulsive hand movements such as wringing and washing follow the loss of functional use of the hands. Over time, most girls affected with Rett syndrome will lose most of their ability to perform ordinary activities; even eye gaze and speech are affected. Rett syndrome looks similar to other autism spectrum disorders, though loss of muscle tone is far more common in Rett syndrome than in other autism spectrum disorders. While the cause of most autism spectrum disorders is unknown, researchers have discovered the cause of Rett syndrome. About 80% of girls affected have a genetic mutation, and a genetic test can confirm the diagnosis. The test involves searching for the MECP2 mutation on the child's X chromosome.

66. Rett Syndrome Rett syndrome — Comprehensive overview covers symptoms, causes and diagnosis of this rare genetic disorder. http://www.cnn.com/HEALTH/library/rett-syndrome/DS00716.html

67. Rett Syndrome: Your Child: University Of Michigan Health System Rett Syndrome. What is Rett syndrome? Rett syndrome is a genetic syndrome that causes autismlike symptoms in girls usually starting between six months and three years of age. http://www.med.umich.edu/yourchild/topics/rett.htm

68. Rett.com Rett Syndrome Magazine offers wisdom, news, and inspiration for the Rett Syndrome community. http://www.rettsyndrome.info/index.html

69. NIH Office Of Rare Diseases Research (ORDR) - Error A US Department of Health and Human Service project providing information on genetic and rare diseases. A comprehensive body of resources on Rett syndrome http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&diseaseID=5696

70. Rett's Syndrome: EMedicine Pediatrics: Developmental And Behavioral Overview Rett syndrome (RS) is a pervasive developmental disorder first reported in 1966 by Andreas Rett, an Austrian pediatric neurologist. Rett syndrome occurs almost http://emedicine.medscape.com/article/916377-overview

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 4     61-70 of 70    Back | 1  | 2  | 3  | 4