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         Usher Syndrome:     more books (26)
  1. Usher's Syndrome: What It Is, How to Cope, and How to Help by Earlene Duncan, Hugh T. Prickett, 1988-07
  2. The Official Patient's Sourcebook On Usher Syndrome: Directory For The Internet Age by Icon Health Publications, 2004-03-31
  3. The Madness of Usher's: Coping With Vision and Hearing Loss/UsherSyndrome Type II (Business of Living Series) by Dorothy H. Stiefel, Richard A. Lewis, 1991-02
  4. Acadian usher syndrome.: An article from: The Proceedings of the Louisiana Academy of Sciences by John P. Doucet, Mary Z. Pelias, et all 1999-01-01
  5. Usher Syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Pamela, MS, CGC Nutting, 2005
  6. Usher syndrome: Identification and understanding by Lisa E Poff, 2000
  7. Otology: Hearing Impairment, Tinnitus, Cochlear Implant, Hearing Aid, Usher Syndrome, Pure Tone Audiometry, Otitis Externa, Balance Disorder
  8. Usher Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  9. Screening for Usher syndrome a hands-on guide for school nurses (SuDoc ED 1.310/2:437763) by Joan Houghton, 1999
  10. Considerations in diagnosing Usher's syndrome: RP and hearing loss by McCay Vernon, 1982
  11. Usher syndrome in the school setting by Ilene Miner, 1998
  12. Usher's syndrome: Deafness and progressive blindness : clinical cases, prevention, theory and literature survey by McCay Vernon, 1969
  13. Questions & answers for the person with Usher's Syndrome by Natalie Powell, 1985
  14. Usher's syndrome: CNS defects determined by computed tomography by Thomas D Bloom, 1983

101. Usher Syndrome - Genetics Home Reference
usher syndrome is a genetic condition characterized by hearing loss and The signs and symptoms of usher syndrome vary in their severity and age of onset
http://ghr.nlm.nih.gov/condition=ushersyndrome
Home What's New Browse Handbook ... Search Usher syndrome
Usher syndrome
On this page:
What is Usher syndrome?
Usher syndrome is a genetic condition characterized by hearing loss and progressive vision loss. The signs and symptoms of Usher syndrome vary in their severity and age of onset; most are present from birth or shortly thereafter, while a few begin later in childhood or adolescence. Genetic changes are related to the following types of Usher syndrome. All types of Usher syndrome include progressive vision loss due to retinitis pigmentosa, a disorder that affects the retina (the part of the eye that detects light and color). Retinitis pigmentosa causes light-sensing cells in the retina to gradually deteriorate. Night vision loss begins first, followed by blind spots that develop in the side (peripheral) vision. These spots enlarge and merge into a doughnut shape, producing tunnel vision. Central vision is reduced and blurs; in some cases, it may be limited but sharp for many years. Cataracts may develop in the teenage years or in adulthood. In addition, some people with Usher syndrome type I or type III have balance problems due to a defect in the part of the inner ear that controls balance.

102. Fondation Jade Champagne Provost
Association autour du syndrome d'usher. Pr©sente ses activit©s, quelques informations sur la maladie, l'©tat de la recherche et des liens s©lectionn©s. Qu©bec.
http://www.fondationjade.com

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103. Australian DeafBlind Council
Information on usher's syndrome. Membership includes people with deafblindness, family, carers, support workers, professionals and service organisations.
http://home.connexus.net.au/~dba/
Welcome to the home page of the Australian DeafBlind Council
PO Box 1213
Camberwell Victoria Australia 3124
Telephone: Voice (03) 9439-2570
Fax (03) 9486 2092 ( +61 39 486 2092)
Email: Australian DeafBlind Council
At This Site
Introduction to Australian DeafBlind Council
Deafblind Interpreting Guidelines: Download Word 97 version
Papers from the National Australian Deafblindness Conference 2000
Australian Contacts
Internet and Overseas Contacts
Resource Papers
How to Join the Australian DeafBlind Council Australian DeafBlind Council Committee Members International Deafblindness information "Beacon" newsletters What is Usher Syndrome? Deafblind Interpreting Guidelines Information on Usher syndrome for parents Publications Usher Syndrome Information Kit The Deaf-Blind Association - Victoria Two-handed Manual Alphabet Deafblind Manual Alphabet
Site Visitors.
Page updated 24-1-03

104. Healthfinder® - Usher's Syndrome
Carefully selected government and nonprofit health information on usher s syndrome.
http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=891

105. Syndrome, Usher Definition - Medical Dictionary Definitions Of Popular Medical T
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=16132

106. Tipsheet: Counseling Students Who Have Usher's Syndrome
Tipsheet Counseling Students Who Have usher s syndrome.
http://www.netac.rit.edu/publication/tipsheet/ushers1.html
Return to Tipsheets Index Directory of Professionals in NE Region Financing Your Education NETAC Brochure ... Home
PEPNet Counseling Students Who Have Usher's Syndrome
1 of 4 Usher Syndrome is an autosomal recessive genetic disorder characterized by congenital hearing loss and gradually developing retinitis pigmentosa leading to the loss of vision. Approximately 25,000 people in the United States have some form of Usher Syndrome. Most of these individuals have either Type I (10,000) or Type II (15,000). Type I Usher Syndrome is characterized by profound congenital deafness, vision problems starting in early childhood, and severe balance problems. An individual born with a moderate to severe hearing loss and normal balance characterizes Type II Usher Syndrome. Night blindness for Type II begins at childhood, but many individuals might not be aware of it until late adolescence/early adulthood. Historically, most students with Usher Syndrome Type I attended residential schools and colleges for the deaf, while individuals with Type II attended regular public schools and universities. With the mainstreaming of deaf and hard-of-hearing students brought about by Public Law 94-142, students with both Type I and II Usher Syndrome can be found in all types of educational settings. It is critical for support service personnel and counselors in college/university environments who work with students with Usher SyndromeÐregardless of typeÐto have a good understanding of special issues that arise for these students and to be aware of strategies that will benefit this population. It also is critical that professionals have a good understanding of Usher Syndrome and what it means to be deaf/hard of hearing and to be losing oneÕs vision.

107. Usher's Syndrome And Retinitis Pigmentosa: Hear-it
usher´s syndrome affects both hearing and sight. usher´s syndrome may also be referred to as Retinitis Pigmentosa. usher´s syndrome is a rare disease.
http://www.hear-it.org/page.dsp?page=330

108. SupportPath.com: Usher's Syndrome
SupportPath.com leads you to Internet resources for supportrelated information on hundreds of health, personal, and relationship topics.
http://www.supportpath.com/sl_u/ushers_syndrome.htm
Usher's Syndrome
A genetic condition resulting in mild to severe hearing loss and a gradual loss of vision (usually beginning in adolescence). Also called: Retinitis Pigmentosa (RP), Usher Syndrome Other topics of interest on SupportPath.com:
disABILITIES
Glaucoma Hearing Impairment Visual Impairment / Blindness ... here
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Online Communities / Message Boards...
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Usenet Groups...
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National / International Organizations...
  • UNITED STATES
    The Foundation Fighting Blindness
    Website:
    http://www.blindness.org/
    Description: "The urgent mission of The Foundation Fighting Blindness is to find the causes, treatments, preventions, and cures for retinitis pigmentosa (RP), macular degeneration, Usher syndrome and the entire spectrum of retinal degenerative diseases." View their Usher Syndrome page.
    Date Added: 03/31/2002
Note: Groups are listed alphabetically by U.S. state and then country.

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