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Waardenburg Syndrome: more detail

Waardenburg Syndrome (Gentics and Communication Disorders Series) by Alice Kahn, 2006-07-25

Light-eyed Negroes and the Klein-Waardenburg Syndrome by Jenni Soussi-Tsafrir, 1974-03

The Official Patient's Sourcebook on Waardenburg Syndrome: A Revised and Updated Directory for the Internet Age by ICON Health Publications, 2006-12-05

Waardenburg Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19

Waardenburg syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Scott, MS Polzin, 2005

Waardenburg Syndrome by AliceKahn, 2006-01-01

Vestibular function and additional findings in Waardenburg's syndrome (Acta Oto-Laryngologica/Supplementum) by Richard E Marcus, 1968

Hereditary deafness in the cat: Free amino acid and sugar content in the perilymph by Hans H Elverland, 1977

lists with details

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
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

Extractions: 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
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

Extractions: (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 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
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

Extractions: (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 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
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
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

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

Extractions: Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: 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
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

Extractions: 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.
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
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

Extractions: Search: Summary Information 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
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

Extractions: Waardenburgs 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.
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

Extractions: W Waardenburg Syndrome... Wada Test... WAIS-R... Walker-Warburg Syndrome... Wallonie. Belgique... Warfarin... Washington University School of Medicine... Waterloo Handedness Questionnaire... Ways of Coping Questionnaire-Revised... Weaver Syndrome... Weaver Syndrome : a case without early overgrowth and review of the literature....
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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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® : 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
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/

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