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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

1. NORD - National Organization For Rare Disorders, Inc.
A general discussion about this disorder, followed by further resources.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Waardenburg S

2. Waardenburg Syndrome [NIDCD Health Information]
waardenburg syndrome (WS) is an inherited disorder often characterized by Other individuals with waardenburg syndrome may have unusually brilliant blue
http://www.nidcd.nih.gov/health/hearing/waard.asp
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Waardenburg Syndrome
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Description
Waardenburg syndrome (WS) is an inherited disorder often characterized by varying degrees of hearing loss and changes in skin and hair pigmentation. The syndrome got its name from a Dutch eye doctor named Petrus Johannes Waardenburg who first noticed that people with differently colored eyes often had a hearing impairment. He went on to study over a thousand individuals in deaf families and found that some of them had certain physical characteristics in common. One commonly observed characteristic of Waardenburg syndrome is two differently colored eyes. One eye is usually brown and the other blue. Sometimes, one eye has two different colors. Other individuals with Waardenburg syndrome may have unusually brilliant blue eyes. People with WS may also have distinctive hair coloring, such as a patch of white hair or premature gray hair as early as age 12. Other possible physical features include a wide space between the inner corners of eyes called a broad nasal root. In addition persons with WS may have low frontal hairline and their eyebrows may connect. The levels of hearing loss associated with the syndrome can vary from moderate to profound. Individuals with Waardenburg syndrome may have some or all of the traits of the syndrome. For example, a person with WS may have a white forelock, a patch of white hair near the forehead, and no hearing impairment. Others may have white patches of skin and severe hearing impairment. The severity of the hearing impairment varies among individuals with WS as do changes in the skin and hair.

3. Waardenburg Syndrome
waardenburg syndrome waardenburg syndrome like any disease comes about as a malfunction of one or more of your bodies systems.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. Waardenburg Syndrome - Parents - Boys Town National Research
Genetics and Deafness waardenburg syndrome
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

5. Ten Syndromes Commonly Associated With Hearing Impairment -
(10) waardenburg syndrome Incidence and Prevalence 1 per 4 000 live births.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. Waardenburg Syndrome - Genetics And Deafness - Information On Hearing Loss - Abo
Dr. Waardenburg went on to study other chraacteristics of the syndrome which The waardenburg syndrome (WS) gene affects the body in three primary ways
http://www.boystownhospital.org/Hearing/info/genetics/syndromes/waardenburg.asp
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Information on Hearing Loss - Waardenburg Syndrome
A Dutch eye doctor, P. J. Waardenburg, was the first to notice that some people with two different colored eyes frequently had hearing problems. Dr. Waardenburg went on to study other chraacteristics of the syndrome which is now named after him. The Waardenburg syndrome (WS) gene affects the body in three primary ways: hearing , pigmentation (coloring) of the skin, hair and eyes, and facial structure. Hearing. There is a great deal of variation in the sensorineural hearing loss among people with WS. At least half of those with the gene have no hearing problems. Only about one out of five have a hearing loss severe enough to require some aid to verbal communication. Some with the gene are totally deaf, and others are deaf in one ear, yet have completely normal hearing in the other ear.
Pigmentation
One of the noticeable effects is two different colored eyes (heterochromia irides). Usually, one eye is brown and the other is blue. occassionally, patches of brown and blue are mixed in the same eye. The blue eye color is often described as a "bright" blue. As with hearing loss, not everyone who carries the gene has two different colored eyes. in fact, in some large families with WS there may be only one or two such individuals. However, a person having two different colored eyes is so noteworthy that it almost always automatically raises the question of WS in that family.

7. EMedicine - Waardenburg Syndrome Article By Lyubomir A
waardenburg syndrome waardenburg syndrome is a rare disease characterized by deafness in association with pigmentary anomalies and defects of
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

8. EMedicine - Waardenburg Syndrome : Article By Lynn Bason, MS
waardenburg syndrome waardenburg syndrome (WS) is named after the Dutch ophthalmologist who, in 1947, first described a patient with hearing loss,
http://www.emedicine.com/ped/topic2422.htm
(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease
Waardenburg Syndrome
Last Updated: April 4, 2003 Rate this Article Email to a Colleague Synonyms and related keywords: WS, 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

9. Waardenburg Syndrome [NIDCD Health Information]
. Types of WS. Cause. Research studies. Additional resources......waardenburg syndrome On this page
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. EMedicine - Waardenburg Syndrome : Article By Lyubomir A Dourmishev, M.D., Ph.D.
waardenburg syndrome waardenburg syndrome is a rare disease characterized by deafness in association with pigmentary anomalies and defects of neural
http://www.emedicine.com/derm/topic690.htm
(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Dermatology Pediatric Diseases
Waardenburg Syndrome
Last Updated: July 22, 2005 Rate this Article Email to a Colleague Synonyms and related keywords: WS, Klein-Waardenburg syndrome, Shah-Waardenburg syndrome, Hirschsprung disease, Hirschsprung's disease, deafness, deafmutism, pigmentary anomalies, white forelock, heterochromia iridis, partial albinism, congenital aganglionic megacolon, dystopia canthorum, PAX3, MITF AUTHOR INFORMATION Section 1 of 9 Author Information Introduction Clinical Differentials ... Bibliography
Author: Lyubomir A Dourmishev, M.D., Ph.D. , Assistant Professor, Department of Dermatology, Medical University, Alexander's University Hospital, Sofia, Bulgaria Coauthor(s): Camila K Janniger, MD , Chief of Pediatric and Geriatric Dermatology, Clinical Professor, Dermatology and Clinical Associate Professor, Pediatrics, UMDNJ-New Jersey Medical School Lyubomir A Dourmishev, M.D., Ph.D., is a member of the following medical societies:

11. MedlinePlus Medical Encyclopedia Waardenburg Syndrome
waardenburg syndrome Contents of this page Illustrations. Definition. Causes, incidence, and risk factors. Symptoms. Signs and tests
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12. Waardenberg Syndrome
THE MAIN CHARACTERISTICS of waardenburg syndrome (WS) include a wide bridge of the nose; pigmentary disturbances such as two different colored eyes,
http://www.ncbi.nlm.nih.gov/disease/Waard.html
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catalog of human genes and disorders Information Search the National Institute for Deafness and other Communication Disorders, NIH The Boys Town Research Registry for Hereditary Hearing Loss fostering links between families, clinicians and researchers THE MAIN CHARACTERISTICS

13. Birth Disorder Information Directory - W
BASAL CELL NEVUS SYNDROME; BCNS waardenburg syndrome. List of Sites (Recessive) Anophthalmia Syndrome. See waardenburg syndrome, Type III
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. OMIM - WAARDENBURG SYNDROME, TYPE I; WS1

http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193500

15. Interaction Among SOX10, PAX3 And MITF, Three Genes Altered In
Interaction among SOX10, PAX3 and MITF, three genes altered in waardenburg syndrome Nadege Bondurand , Veronique Pingault
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

16. Interaction Among SOX10, PAX3 And MITF, Three Genes Altered In
Interaction among SOX10, PAX3 and MITF, three genes altered in waardenburg syndrome Nadege Bondurand , Veronique Pingault
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

17. Waardenburg Syndrome - Cause Of Hearing Loss
waardenburg syndrome is one of the more unusual causes of deafness and hearing loss.
http://deafness.about.com/cs/featurescauses/a/waardenburg.htm
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18. YourDictionary.com - 'Welles Orson' To 'voussoir'
w1 n. w2 abbr. W1. W2 abbr. w. W. WA. WAAC. WAAF. Waal. waardenburg syndrome. Wabanaki. Wabash wabble. WAC1 n. WAC2 abbr. wack
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

19. Waardenburg Syndrome
Do you know someone who has waardenburg syndrome? Just updated with the comments of a parent of a child with waardenburg syndrome .
http://deafness.about.com/b/a/049771.htm
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December 11, 2003
Waardenburg Syndrome
Do you know someone who has Waardenburg syndrome? Just updated with the comments of a parent of a child with Waardenburg syndrome.
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20. 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

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