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         Waardenburg Syndrome:     more detail
  1. Waardenburg Syndrome (Gentics and Communication Disorders Series) by Alice Kahn, 2006-07-25
  2. Light-eyed Negroes and the Klein-Waardenburg Syndrome by Jenni Soussi-Tsafrir, 1974-03
  3. The Official Patient's Sourcebook on Waardenburg Syndrome: A Revised and Updated Directory for the Internet Age by ICON Health Publications, 2006-12-05
  4. Waardenburg Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  5. Waardenburg syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Scott, MS Polzin, 2005
  6. Waardenburg Syndrome by AliceKahn, 2006-01-01
  7. Vestibular function and additional findings in Waardenburg's syndrome (Acta Oto-Laryngologica/Supplementum) by Richard E Marcus, 1968
  8. Hereditary deafness in the cat: Free amino acid and sugar content in the perilymph by Hans H Elverland, 1977

21. Klein-Waardenburg Syndrome (www.whonamedit.com)
Kleinwaardenburg syndrome A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness.
http://www.whonamedit.com/synd.cfm/1086.html

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Klein-Waardenburg syndrome Also known as:
Klein’s syndrome
Mende's syndrome II van der Hoeve-Halbertsma-Waardenburg syndrome Van der Hoeve-Halbertsma-Gualdi syndrome van der Hoeve-Waardenburg-Klein syndrome Vogt’s syndrome (Cécile Vogt) Waardenburg's syndrome II Synonyms: Blepharophimosis, dyschromia iridocutanea et dysplasia auditiva (Waardenburg), dyschromia tridocutanea et dysplasia auditiva, dystopia canthi medialis lateroversa, embryonic fixation syndrome, hyperplasia interocularis cum dystopia lateroversa canthi medialis, interoculiiridodermatoauditory dysplasia syndrome, ptosis-epicanthus syndrome. Associated persons: Unknown Gualdi Nicolaas Adolf Halbertsma David Klein Irmgard Mende ... Petrus Johannes Waardenburg Description: A hereditary congenital defect involving pigmentation. It consists of a white forelock, vitiligo, partial or total heterochromic irides, hyperplastic broad high nasal root, lateral displacement of the medial canthi and lacrimal points, hyperplasia of the median portion of the eyebrows, congenital or partial (unilateral) deafness (15-20 % of affected persons). Although the most serious defect in this syndrome is congenital deafness, it is seldom accepted and mentioned by patients. A conspicuous feature is two different coloured eyes.

22. AllRefer Health - Waardenburg Syndrome
waardenburg syndrome information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, tests, support groups
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Definition Waardenburg syndrome is a group of hereditary conditions characterized by deafness and partial albinism (pale skin, hair and eye color).
Broad Nasal Bridge
Sense of Hearing Waardenburg syndrome is inherited as an autosomal dominant trait; only one parent has to pass on the gene for a child to be affected. There are four types of this syndrome. (Type 3 is known as Klein-Waardenburg syndrome; Type 4 is Waardenburg-Shah syndrome.) 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

23. AllRefer Health - Waardenburg Syndrome Diagnosis & Tests
You are here AllRefer.com Health Diseases Conditions waardenburg syndrome Diagnosis, Tests, Signs of waardenburg syndrome. waardenburg syndrome.
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Examination may show various abnormalities, including:
  • lateral displacement of inner canthi (corners of eye) eyebrows flare in the midline broad nasal bridge deafness (may or may not be present) pale to white portions of eye including back of the eye small or under-developed bones of the face white patches of skin
Tests:
  • audiometry (hearing evaluation) genetic testing of the PAX3 gene on chromosome 2q35 genetic testing of the MITF gene (type 2 Waardenburg syndrome) on chromosome 3p13 tests may show that stool doesn't move through the large bowel normally biopsy of the colon may show no neural ganglia (Hirschsprung disease) in type 4 patients genetic testing of the endothelin-3, endothelin receptor B or SOX10 gene in patients with Waardenburg syndrome type 4.

24. GeneReviews: Waardenburg Syndrome Type 1
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.
http://www.genetests.org/query?dz=ws1

25. Waardenburg Syndrome
waardenburg syndrome Important It is possible that the main title of the report waardenburg syndrome is not the name you expected.
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Health Topics Symptoms ... For a Complete Report Waardenburg Syndrome Important It is possible that the main title of the report Waardenburg Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
  • WS
Disorder Subdivisions
  • Waardenburg Syndrome Type I (WS1) Waardenburg Syndrome Type II (WS2) Waardenburg Syndrome Type IIA (WS2A) Waardenburg Syndrome Type IIB (WS2B) Waardenburg Syndrome Type III (WS3) Waardenburg Syndrome Type IV (WS4)
General Discussion In most cases, Waardenburg syndrome is transmitted as an autosomal dominant trait. A number of different disease genes have been identified that may cause Waardenburg syndrome in certain individuals or families (kindreds). Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

26. Waardenburg Syndrome - Medical Dictionary Definitions Of Popular Medical Terms
MedicineNet Home MedTerms medical dictionary AZ List waardenburg syndrome. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=13431

27. Waardenburg Syndrome
waardenburg syndrome is a genetic disorder that may be evident at birth (congenital). National Organization for Rare Disorders, Inc. waardenburg syndrome.
http://www.bchealthguide.org/kbase/nord/nord430.htm
document.write(''); var hwPrint=1; var hwDocHWID="nord430"; var hwDocTitle="Waardenburg Syndrome"; var hwRank="1"; var hwSectionHWID="nord430"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD";
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Waardenburg Syndrome
Important
It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
Synonyms
  • WS
Disorder Subdivisions
  • Waardenburg Syndrome Type I (WS1) Waardenburg Syndrome Type II (WS2) Waardenburg Syndrome Type IIA (WS2A) Waardenburg Syndrome Type IIB (WS2B) Waardenburg Syndrome Type III (WS3) Waardenburg Syndrome Type IV (WS4)
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
  • Cutaneous Albinism and Deafness Cutaneous Albinism without Deafness Harada Syndrome Vogt-Koyanagi Syndrome
General Discussion
In most cases, Waardenburg syndrome is transmitted as an autosomal dominant trait. A number of different disease genes have been identified that may cause Waardenburg syndrome in certain individuals or families (kindreds).

28. Waardenburg Syndrome
waardenburg syndrome. General Discussion. waardenburg syndrome is a genetic disorder that may be evident at birth (congenital). The
http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord430

29. Waardenburg Syndrome
waardenburg syndrome. waardenburg syndrome is an autosomal dominant hereditary condition. It is characterized mainly by lateral (outward
http://www.drhull.com/EncyMaster/W/Waardenburg_syndrome.html

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Encyclopedia Index W Waardenburg syndrome Search
Waardenburg syndrome
Waardenburg syndrome is an autosomal dominant hereditary condition. It is characterized mainly by
  • lateral (outward) displacement of the inner corners of the eyes
  • pigmentary disturbances
    • white forelock in the hair
    • congenital heterochromia of the pupils
    • patches of lighter pigmentation of the skin
  • defective hearing
The linkage of the white forelock with hearing defects means that this feature should logically prompt a hearing evaluation for any baby born with such a forelock.

30. Waardenburg Syndrome Type 3 Information Diseases Database
waardenburg syndrome type 3,Kleinwaardenburg syndrome, Disease Database Information. waardenburg syndrome type 3 aka/or Klein-waardenburg syndrome
http://www.diseasesdatabase.com/ddb33475.htm
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2 synonyms or equivalents were found. Waardenburg syndrome type 3
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31. HealthlinkUSA Waardenburg Syndrome Links
You can find waardenburg syndrome right now at Info.com. Click here for page 1 of waardenburg syndrome information from the HealthlinkUSA directory.
http://www.healthlinkusa.com/332ent.htm

32. Waardenburg Syndrome; Treatment, Prevention, Cure
waardenburg syndromeSearch information from many of the best waardenburg syndrome health sites. Related Searches. waardenburg syndrome message board/forum.
http://www.healthlinkusa.com/content/332.html
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33. Disease Directory : Genetic Disorders : Waardenburg Syndrome
Diseases Genetic Disorders waardenburg syndrome. AllRefer Health Waardenburg of waardenburg syndrome. waardenburg syndrome.
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34. Waardenburg Syndrome
Back Home Next. waardenburg syndrome. NORD waardenburg syndrome. waardenburg syndrome. waardenburg syndromes. Syndromic Hearing Loss.
http://www.ability.org.uk/Waardenburg_Syndrome.html
"see the ability, not the disability" You to can help support the Ability Project by: Our Aims ... Z Waardenburg Syndrome NORD - Waardenburg Syndrome Waardenburg Syndrome Waardenburg Syndromes Syndromic Hearing Loss ... Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

35. KLEIN-WAARDENBURG SYNDROME
Features Listed For waardenburg syndrome. McKusick 193500. Anal atresia/stenosis; Carpal synostosis; Cleft palate; Cleft upper lip (nonmidline);
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1776

36. 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

37. Waardenburg Syndrome
waardenburg syndrome. waardenburg syndrome like any disease comes about as a 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.

38. Genetic Disorders, Waardenburg Syndrome
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39. Waardenburg Syndrome- Medcohealth.com
waardenburg syndrome is a group of hereditary conditions characterized by deafness and partial albinism (pale skin, hair and eye color). waardenburg syndrome.
http://www.medcohealth.com/medco/consumer/ehealth/ehsarticle.jsp?topicID=HE:Dise

40. Health Library -
waardenburg syndrome. Important It is possible that the main title of the report waardenburg syndrome is not the name you expected.
http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

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