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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

81. Qango : Health: Diseases And Conditions: W: Waardenburg Syndrome
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82. Deafness/Hearing Impairment: Waardenburg Syndrome
Dear Lynda, Thank you and I will answer your question best I can. It is rare, waardenburg syndrome (WS) is an inherited disorder often characterized by
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Topic: Deafness/Hearing Impairment
Expert: Dr. Jerry Martin, Ed.D.
Date: Subject: Waardenburg syndrome Question Several medical genetiticist diagnosed me with Waardenburg syndrome two. How rare is waardenburg syndrome two? Thank you for your time and information. Wishing you well personally and professionally. My personal site is http://disabilityinfo.2ya.com Answer Dear Lynda, Thank you and I will answer your question best I can. It is rare, 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.

83. Waardenburg Syndrome - Definition Of Waardenburg Syndrome In The Medical Diction
Definition of waardenburg syndrome in the Medical Dictionary and Thesaurus. waardenburg syndrome explanation. Information about waardenburg syndrome in Free
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Cite / link Email Feedback Waar·den·burg syndrome (wôr dn-bûrg , vär n. An inherited syndrome marked by displacement of the medial canthi and lacrimal puncta, a broad nasal bridge, multicolored or hyperpigmented irises, cochlear deafness, and a white forelock. Mentioned in No references found Medical browser Full browser vulvitis vulvo- vulvovaginal vulvovaginitis ... w/u Waardenburg syndrome Wagner von Jauregg waist waist of heart Waksman ... WAAR Waardenburg syndrome Waardenburg's syndrome Waardenburg's syndrome Waaree Instrument Calibration Laboratory Waarnemend ... WABAC Word (phrase): Word Starts with Ends with Definition Free Tools: For surfers: Browser extension Word of the Day NEW!

84. Expert - Waardenburg Syndrome
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85. Speakers Bureau - Waardenburg Syndrome
Speakers Bureau Directory Find motivational business leaders and legal professionals speakers in waardenburg syndrome for all events.
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86. Waardenburg Syndrome Synonyms, Eastern Carolina
waardenburg syndrome Synonyms University Health Systems of Eastern Carolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county,
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Waardenburg Syndrome
Synonyms
Disorder Subdivisions

General Discussion

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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

87. HONselect - Waardenburg's Syndrome
Syndrome - Waardenburg-Klein Syndrome - Klein Syndrome - Klein waardenburg syndrome - Kleins Syndrome. Français, Syndrome de Waardenburg
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English: Waardenburg's Syndrome - Klein-Waardenburg Syndrome
- Klein's Syndrome
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- Klein Syndrome
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Français: Syndrome de Waardenburg - Syndrome de Waardenburg de type III - Syndrome de Klein - Syndrome de Klein-Waardenburg - Syndrome de Waardenburg de type 3 Deutsch: Waardenburg-Syndrom - Klein-Waardenburg-Syndrom Español: Síndrome de Waardenburg - Síndrome de Klein Waardenburg Português: Síndrome de Waardenburg - Síndrome de Klein Waardenburg HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: No Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C16.131.077.938.html Last modified: Wed May 18 2005

88. Health And Wellness Dictionary: Waardenburg Syndrome
waardenburg syndrome. Hereditary disorder that is characterized by hearing impairment, a white shock of hair and/or distinctive blue color to one or both
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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.
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89. Page Not Found - Boys Town National Research Hospital
Information About Usher syndrome Insights from our Research Leaders http//www.boystownhospital.org80/parents/info/genetics/waardenburg.asp
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90. Waardenburg's Syndrome III (www.whonamedit.com)
waardenburg s syndrome III A hereditary syndrome characterized by anophthalmia and limb abnormalities, mainly syndactyly. Also known as waardenburg s
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Waardenburg's syndrome III Also known as: Waardenburg's anophthalmia syndrome Synonyms: Anophthalmos-syndactyly syndrome. Associated persons: Petrus Johannes Waardenburg Description: A hereditary syndrome, transmitted as an autosomal recessive trait, characterized by anophthalmia and limb abnormalities, mainly syndactyly. Bibliography:
  • P. J. Waardenburg: Autosomal-recessive anophthalmia with malformations of the hands and feet. In: P. J. Waardenburg, A. Franceschetti, D. Klein (editors): Genetics in ophthalmology. Assen, Royal van Gorcum, 1961, v. 1, p. 773.
Ole Daniel Enersen

91. National Deaf Children S Society - Waardenburg S Syndrome
An NDCS factsheet providing information for parents on waardenburg s syndrome.
http://www.ndcs.org.uk/information/childhood_deafness/waardenburgs_syndrome/
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Waardenburg's syndrome
An NDCS factsheet providing information for parents on Waardenburg's syndrome. To view this NDCS publication click on the link below: Waardenburg's syndrome (April 2003) (169 kb) To download and read this publication you will need Adobe Reader, which can be downloaded simply and free of charge from the Adobe website Parent Place Would you like to discuss issues and share experiences with other parents? Why not visit Parent Place, the NDCS online forum for parents, to join in the discussions on a whole range of topics. Visit Parent Place Would you like to comment on this NDCS publication? Has this NDCS publication been useful to you or could we improve it somehow? We are constantly updating existing publications and adding new ones to our list and would love to hear from you if you think there is anything we could do better. Please use the 'Post comment' function on the right of the page to send us your comments. Thanks!

92. National Deaf Children S Society - Waardenburg S Syndrome
NDCS factsheet for parents on waardenburg s syndrome.
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93. Waardenburg Syndrome Type 1 Information Diseases Database
waardenburg s syndrome type 1, Disease Database Information.
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94. Waardenburg’s Syndrome Kharya AV, Agarwal SN - Indian J Dermatol Venereol Lepro
waardenburg s syndrome is an autosomal dominant, rare disorder of neural There are three types of waardenburg s syndrome indicating genetic heterocity.
http://www.ijdvl.com/article.asp?issn=0378-6323;year=2003;volume=69;issue=7;spag

95. Syndrome De Waardenburg : Sites Et Documents Francophones
Translate this page waardenburg type 2, syndrome de - synonymes waardenburg type 2A, waardenburg type 3, syndrome de - synonyme Klein-waardenburg, syndrome de
http://www.chu-rouen.fr/ssf/pathol/waardenburgsyndrome.html
Syndrome de Waardenburg Synonyme(s) CISMeF Klein-Waardenburg, syndrome de ; Waardenburg ; Waardenburg type 2A, syndrome de ; Waardenburg type 2B, syndrome de ; Waardenburg type 4, syndrome de ; waardenburg, syndrome .
Synonyme(s) MeSH Syndrome de Klein ; Syndrome de Klein-Waardenburg ; Syndrome de Waardenburg de type 3 ; Syndrome de Waardenburg de type III
Voir aussi mégacôlon congénital
Arborescence(s) syndrome de Waardenburg waardenburg's syndrome
maladies et malformations congénitales, héréditaires et néonatales
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96. Waardenburg's Syndrome - Definition Of Waardenburg's Syndrome In The Medical Dic
Definition of waardenburg s syndrome in the Medical Dictionary and Thesaurus. waardenburg s syndrome explanation. Information about waardenburg s syndrome
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Waardenburg syndrome (redirected from Waardenburg's syndrome
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Cite / link Email Feedback Waar·den·burg syndrome (wôr dn-bûrg , vär n. An inherited syndrome marked by displacement of the medial canthi and lacrimal puncta, a broad nasal bridge, multicolored or hyperpigmented irises, cochlear deafness, and a white forelock. Mentioned in No references found Medical browser Full browser vulvo- vulvovaginal vulvovaginitis W ... Waardenburg syndrome Waardenburg's syndrome Wagner von Jauregg waist waist of heart Waksman ... Waardenburg syndrome Waardenburg's syndrome Waaree Instrument Calibration Laboratory Waarnemend WAARNG WAARS ... Waart, Edo de

97. DermIS / Menu Principal / PeDOIA / Table Des Matières / 12 Anomalies de la 
syndrome de waardenburg Si vous êtes un patient avec syndrome de waardenburg SVP, complétez notre
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98. Waardenburg's Syndrome Patients Have Mutations In The Human Homologue Of The Pax
waardenburg s syndrome patients have mutations in the human homologue of the Pax3 paired box gene. Mayada Tassabehji*, Andrew P. Read*†, Valerie E. Newton‡
http://dx.doi.org/10.1038/355635a0
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Nature , 635 - 636 (13 February 1992); doi:10.1038/355635a0 Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Mayada Tassabehji , Andrew P. Read , Valerie E. Newton , Rodney Harris , Rudi Balling , Peter Gruss University Department of Medical Genetics, St Mary's Hospital, Manchester M13 OJH, UK
Centre for Audiology, University of Manchester, Oxford Road, Manchester M13 9PL, UK.
Max Planck Institute for Immunobiology, D-7800 Freiburg, Germany.
To whom correspondence should be addressed.
WAARDENGURG'S syndrome (WS) is an autosomal dominant combination of deafness and pigmentary disturbances, probably caused by defective function of the embryonic neural crest . We have mapped one gene for WS to the distal part of chromosome 2 (ref. 3). On the basis of their homologous chromosomal location, their close linkage to an alkaline phosphatase gene, and their related phenotype, we suggested that WS and the mouse mutant Splotch might be homologous.

99. Waardenburg's Syndrome - General Practice Notebook
waardenburg s syndrome. waardenburg s syndrome is the association of. patchy depigmentation of the skin; sensorineural deafness; a white forelock
http://www.gpnotebook.co.uk/cache/-1462763481.htm
Waardenburg's syndrome Waardenburg's syndrome is the association of:
  • patchy depigmentation of the skin sensorineural deafness a white forelock unusual facial hair distribution - fusion of the eyebrows in the midline heterochromia of the iris bilateral displacement of the medial canthi

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100. MeSH-D Terms Associated To MeSH-C Term Waardenburg S Syndrome
MeSHD terms associated to MeSH-C term waardenburg s syndrome, G2D Home strength of the association of the corresponding term to waardenburg s syndrome.
http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Waardenburg's_Syndrome:unknown

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