21. Health Library - Waardenburg Syndrome waardenburg syndrome. Synonyms Disorder time. waardenburg syndrome isa genetic disorder that may be evident at birth (congenital). The http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

22. Waardenburg Syndrome - Cause Of Hearing Loss waardenburg syndrome Cause of Hearing Loss. Black and white streakedhair equals Waardenburg. Join the Discussion. My one year old http://deafness.about.com/library/weekly/aa080398.htm

zfp=-1 About Deafness/Hard of Hearing Search in this topic on About on the Web in Products Web Hosting Deafness/Hard of Hearing with Jamie Berke Your Guide to one of hundreds of sites Home Articles Forums ... Help zmhp('style="color:#fff"') Subjects ESSENTIALS FAQ on Deafness and Hearing Loss Sign Language Glossary Feature Article Index ... All articles on this topic Stay up-to-date! Subscribe to our newsletter. Advertising Free Credit Report Free Psychics Advertisement Waardenburg Syndrome - Cause of Hearing Loss Black and white streaked hair equals Waardenburg Join the Discussion "My one year old daughter was recently diagnosed as being deaf. After taking her to a genetics specialist to see why they diagnosed her and my husband with Waardensburg Syndrome." Got Waardenburg? Related Resources Etiology subject page I had heard of Waardenburg Syndrome but had never actually seen it until one day in college I met a girl whose hair was black and streaked with white. As rare as it is, I have had e-mails from families seeking information on Waardenburg. What are the characteristics of Waardenburg? First, both eyes may be of a different color. A person could have one blue eye and one brown eye. While it may cause hearing loss, only one out of five people with Waardenburg are hearing impaired enough to need amplification. There are other features, such as spacing of the eyes, but they are really quite minor - so minor that Waardenburg sometimes is not identified. According to the NIDCD

23. EMedicine - Waardenburg Syndrome : Article By Lyubomir A Dourmishev, MD waardenburg syndrome waardenburg syndrome is a rare disease characterized bydeafness in association with pigmentary anomalies and defects of neural crest http://www.emedicine.com/derm/topic690.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Dermatology Pediatric Diseases Waardenburg Syndrome Last Updated: December 26, 2001 Rate this Article Email to a Colleague Synonyms and related keywords: Klein-Waardenburg syndrome AUTHOR INFORMATION Section 1 of 9 Author Information Introduction Clinical Differentials ... Bibliography Author: Lyubomir A Dourmishev, MD , Assistant Professor, Department of Dermatology, Alexander's University Hospital, Sofia, Bulgaria Coauthor(s): Camila K Janniger, MD , Chief of Pediatric and Geriatric Dermatology, Clinical Associate Professor, Dermatology and Pediatrics, UMDNJ-New Jersey Medical School Editor(s): Albert C Yan, MD , Assistant Professor, Department of Pediatrics, Section of Dermatology, Children's Hospital of Philadelphia and University of Pennsylvania; Richard Vinson, MD , Chief, Department of Dermatology, William Beaumont Medical Center; Robert A Schwartz, MD, MPH

24. EMedicine - Waardenburg Syndrome : Article By Lynn Bason, MS waardenburg syndrome waardenburg syndrome (WS) is named after the Dutch ophthalmologistwho, in 1947, first described a patient with hearing loss, dystopia http://www.emedicine.com/ped/topic2422.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Waardenburg Syndrome Last Updated: July 10, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: WS1, WS2, Klein-Waardenburg syndrome, WS3, Waardenburg-Shah syndrome, WS4 AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Lynn Bason, MS , Genetic Counselor, Department of Clinical Genetics, Division of Human Genetics, Children's Hospital of Philadelphia Coauthor(s): Ian Krantz, MD , Assistant Professor, Department of Pediatrics, University of Pennsylvania and Children's Hospital of Philadelphia Lynn Bason, MS, is a member of the following medical societies: American Society of Human Genetics Editor(s): Erawati Bawle, MD, FAAP, FACMG , Director, Division of Genetic and Metabolic Diseases, Children's Hospital of Michigan; Clinical Professor, Department of Pediatrics, Wayne State University School of Medicine; Robert Konop, PharmD

25. Health Library - Waardenburg Syndrome waardenburg syndrome. Synonyms Disorder time. waardenburg syndrome isa genetic disorder that may be evident at birth (congenital). The http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid

26. Waardenburg Syndrome waardenburg syndrome. waardenburg syndrome like any disease comes about asa malfunction of one or more of your bodies systems. waardenburg syndrome. http://www.tjclarkinc.com/d_waardenburg_syndrome.htm

Waardenburg Syndrome Waardenburg Syndrome like any disease comes about as a malfunction of one or more of your bodies systems. Much if not most of the time this is a result of a slow degenerative process due to the lack of adequate bodily supplies of the elements necessary for normal function and rejuvenation of affected organs. Commercial Farming and natural erosion has depleted global farmlands of most essential elements therefore it is not wise to assume that your diet contains enough of these elements for normal body function and maintenance. See Senate Document 264. It is also unwise to suspect that intervention therapies will be successful without adequate dietary levels of these elements in useable forms. See The Package. Does what you eat provide all the essential elements you need? See Senate Document 264.

27. Waardenburg Syndrome waardenburg syndrome. waardenburg syndrome Information. More WaardenburgSyndrome Information. and more waardenburg syndrome Information. HOME. http://www.communicationdisorders.net/Waardenburg syndrome.html

Waardenburg syndrome Waardenburg Syndrome Information More Waardenburg Syndrome Information and more Waardenburg Syndrome Information HOME

28. Health Library - Waardenburg Syndrome Saint Luke's Health System eLibrary. waardenburg syndrome. waardenburg syndromeis a genetic disorder that may be evident at birth (congenital). http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h

29. KLEIN-WAARDENBURG SYNDROME Features Listed For KLEINwaardenburg syndrome. McKusick 148820. Blepharophimosis/blepharospasm;Camptodactyly; Camptodactyly/hammer toes; Carpal synostosis; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?932

30. KLEIN-WAARDENBURG SYNDROME Features Listed For HIRSCHSPRUNG DISEASE WITH waardenburg syndrome FEATURES.McKusick 277580. Deafness, sensorineural; Dystopia canthorum http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?774

31. MEDLINEplus Medical Encyclopedia: Waardenberg Syndrome waardenburg syndrome affects about 1 in 30,000 people. Almost 90%of patients have an affected parent but the manifestations of http://www.nlm.nih.gov/medlineplus/ency/article/001428.htm

Skip navigation Medical Encyclopedia Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Waardenberg syndrome Contents of this page: Illustrations Alternative names Definition Causes, incidence, and risk factors ... Prevention Illustrations Broad nasal bridge Sense of hearing Alternative names Return to top Waardenberg syndrome types 1-4; Type 3 = Klein-Waardenberg syndrome; Type 4 = Waardenburg-Shah syndrome Definition Return to top A group of heritable conditions, which include deafness and partial albinism (pale skin, hair and eye color) as their most important features. Causes, incidence, and risk factors Return to top Waardenberg syndrome is inherited as an autosomal dominant trait; only one parent has to pass on the gene for a child to be affected. The multiple types of this syndrome result from mutations occurring in different genes. All types share two dominant features: hearing loss and partial albinism . The albinism is incomplete and may appear as a white forelock in an otherwise dark head of hair, very pale light blue eyes, or two

32. Health And Wellness Dictionary: Waardenburg Syndrome Dictionary Contents W waardenburg syndrome. Health and WellnessDictionary Definition. waardenburg syndrome. Hereditary disorder http://geoparent.com/dictionary/Detailed/365.htm

From pre-pregnancy to baby care through parenting... See more from GeoParent! Parenting features GeoParent Local ePregnancy Chef Mom.com Myria - for moms SheKnows directory HolidayNotes webcards search site directory local sites message boards ... main page Search: site directory more search options Dictionary Contents W : Waardenburg Syndrome Health and Wellness Dictionary: Definition Dictionary Main Search GeoParent Main Page Health articles ... X-Y-Z Waardenburg Syndrome Hereditary disorder that is characterized by hearing impairment, a white shock of hair and/or distinctive blue color to one or both eyes, and wide-set inner corners of the eyes. Balance problems are also associated with some types of waardenburg syndrome. Want more? Click here to search the rest of the GeoParent site for information on Waardenburg Syndrome! Search the dictionary Click for more search options Look it up in our health dictionary! The Vegetarian Child (book) Check out our local features! Directory of Health Articles Directory of all articles About this information: These definitions were provided by the Centers for Disease Control, the National Institutes for Health and other government health agencies. This information is for educational purposes only. If you are concerned about your health or your child's health, please consult your family's health care provider immediately. This information is not a substitute for personal medical attention, diagnosis or treatment.

33. NORD - National Organization For Rare Disorders, Inc. waardenburg syndrome. To purchase fulltext report ($7.50) View Cart/Checkout.Copyright 1987, 1988, 1989, 1993, 2000 Synonyms of waardenburg syndrome WS. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Waardenburg S

34. PAX3 - Paired Box Homeotic Gene 3 (Waardenburg Syndrome 1) - Aka: WS1, HUP2 - Ca Summary Information. PAX3; Paired box homeotic gene 3 (Waardenburgsyndrome 1). Location 2q35. Aliases WS1, HUP2. Overview PAX genes http://www.cancerindex.org/geneweb/PAX3.htm

Cancer Genetics Web www.cancer genetics.org ; Paired box homeotic gene 3 (Waardenburg syndrome 1) (2q35) PAX3 Menu Summary Information - PAX3 Gene Database Entries for PAX3 Other PAX3 Related Resources t(2;13)(q35;q14) in Rhabdomyosarcoma ... Feedback / suggest a new topic for PAX3 Search: Summary Information PAX3; Paired box homeotic gene 3 (Waardenburg syndrome 1) Location: Aliases: Overview: PAX genes are a family of transcription factors essential to the genesis of a variety of tissues and organs. Mutations leading to a loss of function in PAX3 are found in people with Waardenburg Syndrome indicating that PAX3 is necessary for the correct formation of caudal neural crest derivatives and for the migration of myoblasts into the limbs. Mutations of PAX3 leading to gain of function when fused with the FKHR gene (another transcription factor) are associated with alveolar rhabdomyosarcomas. Return to PAX3 Contents Gene Database Entries for PAX3 OMIM GeneCard (Weizmann Institute) Human Gene Mutation Database (Cardiff, UK) Locus Link UniGene GenAtlas GDB ... Nomenclature (search for PAX3) Return to PAX3 Contents Other Related Resources Search Medline for related articles (PubMed) Medline Search: cancer AND gene AND (PAX3[TI] OR WS1[TI] OR HUP2[TI]) (PubMed) Limit search to: [Last Year] Limit search to: [Last 2 Years] Limit search to: [Reviews] Return to PAX3 Contents t(2;13)(q35;q14) in Rhabdomyosarcoma

35. WAARDENBURG SYNDROME waardenburg syndrome. Int J Dermatol 1999;3865663. Transcription factor hierarchyin waardenburg syndrome regulation of MITF expression by SOX10 and PAX3. http://www.med.wayne.edu/dermatology/MichDerm Online 2002/31WAARDENBURG SYNDROME

CASE 31—WAARDENBURG’S SYNDROME Waardenburg’s Syndrome (WS) is a rare autosomal dominant syndrome characterized by pigmentary disturbances (skin, hair, iris), sensorineural hearing loss, and other developmental anomalies such as dystopia canthorum and blepharophimosis. Patients may not present with all clinical manifestations. WS occurs in 1/42,000 of the general population and 2% of the congenitally deaf population. The hearing loss in WS is sensorineural, may be unilateral or bilateral, and varies in severity. Dystopia canthorum is the most penetrant feature of WS type I; present in 99% of cases. The W index objectively diagnoses lateral displacement of the inner canthi. To calculate the W index: (1) Measure a, b, and c in mm; (2) Calculate X = (2a - 0.2119c - 3.909)/c; (3) Calculate Y = (2a - 0.2479b – 3.909)/b; (4) Calculate W = X + Y + a/b. WS type I is diagnosed if the average W of all affected family members is Pigmentary abnormalities of hair include a white forelock or premature graying. The white forelock may be present at birth or soon after.

36. AD HOC BIBLIO - INDEX SUJETS LETTRE W Compilé Le 14/01/03 INDEXSUJETS , Lettre W waardenburg syndrome Childhood strokeafter minor neck trauma case report .a; Wada Test Aphasie http://www.cidg.com/~marienf/k/i/mid1w.htm

W Waardenburg Syndrome... Childhood stroke after minor neck trauma: case report.... [a] Wada Test... [a] Intracarotid amobarbital testing in presurgical evaluation of patients with epil... [a] WAIS-R... Normative data on the validity of Canadian subsitute items for the WAIS-R Inform... [a] Walker-Warburg Syndrome... [a] Inflammatory myopathy and Walker-Warburg Syndrome: etiologic implications.... [a] Merosin-deficient congenital muscular dystrophy : the spectrum of brain involvme... [a] Wallonie. Belgique... [m] Warfarin... Warfarin resistance and enteral feeding : 2 case reports and a supporting in vit... [a] Washington University School of Medicine... Brachial Plexus... [a] Neuroscience tutorial. An illustrated guide to the essential basics of clinical ... [m] Waterloo Handedness Questionnaire... Factorial structure of the Waterloo Handedness Questionnaire for control and lea... [a] Ways of Coping Questionnaire-Revised... Coping following traumatic brain injury (TBI): derivation and validation of TBI ... [a] Weaver Syndrome... Weaver Syndrome : a case without early overgrowth and review of the literature....

37. Experts, Consultants, Authorities - Waardenburg Syndrome Specialty waardenburg syndrome. Physicians For Quality. 1017 W. HopkinsSan Marcos, Texas 78666 Tel 800284-3627, Fax 512-805-8358 http://www.hgexperts.com/listing/Medical-Experts-Waardenburg-Syndrome.asp

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38. ORPHANET® : Waardenburg Syndrome Type 2 Translate this page ORPHANET. ORPHANET database access. waardenburg syndrometype 2. Direct access to details Alias Home Page. http://www.orpha.net/static/GB/waardenburg_type_2.html

ORPHANET database access Waardenburg syndrome type 2 Direct access to details Alias : Home Page

39. ORPHANET® : Waardenburg Syndrome Type 3 Translate this page ORPHANET. ORPHANET database access. waardenburg syndrome type 3. Directaccess to details Alias Klein-waardenburg syndrome. Home Page. http://www.orpha.net/static/GB/waardenburg_type_3.html

ORPHANET database access Waardenburg syndrome type 3 Direct access to details Alias : Home Page

40. GeneReviews: Waardenburg Syndrome Type 1 Your browser does not support HTML frames so you must view waardenburg syndromeType 1 in a slightly less readable form. Please follow this link to do so. http://www.geneclinics.org/profiles/ws1/

Your browser does not support HTML frames so you must view Waardenburg Syndrome Type 1 in a slightly less readable form. Please follow this link to do so.

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