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waardenburg's syndrome - inherited disease causing hearing loss and pigment changes
Definition for Waardenburg's Syndrome
Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes.
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Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes. Although most people with Waardenburg syndrome have normal hearing, moderate to profound hearing loss can occur in one or both ears. People with this condition often have very pale blue eyes or different colored eyes, such as one blue eye and one brown eye. Sometimes one eye has segments of two different colors. Distinctive hair coloring (such as a patch of white hair or hair that prematurely turns gray) is another common sign of the condition. The features of Waardenburg syndrome vary among affected individuals, even among people in the same family.
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some common symptoms
face deformities
premature graying of hair
white patches on eyeballs
widely spaced eyes
some related diagnoses
1 - 7 of
40
diagnoses
Noonan's Syndrome
Pfeiffer Syndrome
DiGeorge's Syndrome
fibrous dysplasia of bone
hypertelorism
nasal polyp
hereditary orotic aciduria
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do i have 'Waardenburg's Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'waardenburg's syndrome'
1 - 5 of
9
diagnostic tests
Molecular Genetic Studies
Waardenburg's Syndrome and Molecular Genetic Studies
Hearing test
standard technique of representing hearing loss
Waardenburg's Syndrome and Hearing test
vision tests
Waardenburg's Syndrome and vision tests
CT inner ear
Waardenburg's Syndrome and CT inner ear
CT scan
Waardenburg's Syndrome and CT scan
CT temporal bone(s)
Waardenburg's Syndrome and CT temporal bone(s)
Comprehensive eye exam
Waardenburg's Syndrome and Comprehensive eye exam
Developmental testing
Waardenburg's Syndrome and Developmental testing
speech reception threshold (SRT)
Waardenburg's Syndrome and speech reception threshold (SRT)
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therapeutic procedures for 'Waardenburg's Syndrome'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Waardenburg's Syndrome:
therapeutic procedure search results for 'waardenburg's syndrome'
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rankings are computer generated. please consult your health care provider.
Special Education
Waardenburg's Syndrome and Special Education
Speech Therapy
Waardenburg's Syndrome and Speech Therapy
medications search results for 'waardenburg's syndrome'
rankings are computer generated. please consult your health care provider.
web search results for waardenburg's syndrome
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1 - 50
- Waardenburg's Syndrome
Waardenburg's syndrome.
1: Indian J Ophthalmol. 1980 Apr;28(1):37-8. Waardenburg's syndrome. Joseph TA, Chakravarthy KS. ... Waardenburg's Syndrome/diagnosis. Waardenburg's Syndrome/genetics ...
http://www.ncbi.nlm.nih.gov/pubmed/7203595?ordinalpos=72&ito...
www.ncbi.nlm.nih.gov
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Waardenburg's syndrome.
1: Cutis. 1978 May;21(5):685-6. Waardenburg's syndrome. Poche GW, Christianson HB. ... Nose/abnormalities. Waardenburg's Syndrome/diagnosis* PMID: 417897 ...
http://www.ncbi.nlm.nih.gov/pubmed/417897
www.ncbi.nlm.nih.gov
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Waardenburg syndrome
Waardenburg syndrome is a group of hereditary conditions characterized by ... Waardenburg syndrome affects about 1 in every 30,000 people. ...
http://adam.about.com/encyclopedia/infectiousdiseases/Waardenburg-syndrome.htm
adam.about.com
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ABCD syndrome - Wikipedia, the free encyclopedia
Waardenburg decided to define the syndrome with the six major symptoms that ... This helped them distinguish different forms of Waardenburg syndrome. ...
http://en.wikipedia.org/wiki/ABCD_syndrome
en.wikipedia.org
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Waardenburg syndrome - Genetics Home Reference
... known types of Waardenburg syndrome are distinguished by their ... Mutations in the EDN3, EDNRB, MITF, PAX3, SNAI2, and SOX10 genes cause Waardenburg syndrome. ...
http://ghr.nlm.nih.gov/condition=waardenburgsyndrome
ghr.nlm.nih.gov
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MedlinePlus Medical Encyclopedia: Waardenburg syndrome
Waardenburg syndrome is a group of hereditary conditions characterized by ... Waardenburg syndrome affects about 1 in every 30,000 people. ...
http://www.nlm.nih.gov/medlineplus/ency/article/001428.htm
www.nlm.nih.gov
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Genetic heterogeneity in the Waardenburg syndrome.
Genetic heterogeneity in the Waardenburg syndrome. Arias S. ... Waardenburg's Syndrome/pathology. PMID: 5006208 [PubMed - indexed for MEDLINE] ...
http://www.ncbi.nlm.nih.gov/pubmed/5006208
www.ncbi.nlm.nih.gov
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Loyola University Health System
Waardenburg syndrome is a group of hereditary conditions characterized by ... Waardenburg syndrome affects about 1 in every 30,000 people. ...
http://loyolauniversity.adam.com/content.aspx?productId=101&pid=1&gid=001428
loyolauniversity.adam.com
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WAARDENBURG SYNDROMES - Pedbase.org
WAARDENBURG ... described in 1951 by Waardenburg in a group of congenitally ... 4. Type III (Klein-Waardenburg limb anomalies) all features above. bilateral ...
http://pedbase.org/w/waardenburg-syndrome/
pedbase.org
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Waardenburg syndrome type II
Waardenburg syndrome type II (WS II): type IIA when linked to locus 3p13; type ... L and Vekemans M. Waardenburg syndrome typeII. Orphanet encyclopedia, May ...
http://www.orpha.net/data/patho/GB/uk-WS2.html
www.orpha.net
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Waardenburg syndrome - Wikipedia, the free encyclopedia
Waardenburg syndrome is named after Dutch ophthalmologist Petrus Johannes ... Waardenburg syndrome has also been associated with a variety of other congenital ...
http://en.wikipedia.org/wiki/Waardenburg_syndrome
en.wikipedia.org
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Search Results
... to get there faster: Go Wa Waardenburg's syndrome Common Craniofacial Syndromes ... Nephrotic syndrome is urinary excretion of > 3 g of. ...
http://www.merck.com/mrksearch/SearchServlet?filtN=professio...
www.merck.com
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Autosomal dominant inheritance of Klein-Waardenburg syndrome.
Autosomal dominant inheritance of Klein-Waardenburg syndrome. Sheffer R, Zlotogora J. ... Male. Waardenburg's Syndrome/genetics* PMID: 1536170 [PubMed ...
http://www.ncbi.nlm.nih.gov/pubmed/1536170
www.ncbi.nlm.nih.gov
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Waardenburg syndrome
Waardenburg syndrome is a group of hereditary conditions characterized by and partial (pale ... MITF gene (type 2 Waardenburg syndrome) on chromosome 3p13 ...
http://adam.about.com/encyclopedia/001428sym.htm
adam.about.com
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Waardenburg syndrome - OMIM - Genetic disorder catalog - Genetics Home ...
... in the Genetics Home Reference condition summary on Waardenburg syndrome. OMIM: Waardenburg syndrome, type I. OMIM: Waardenburg syndrome, type IIA ...
http://ghr.nlm.nih.gov/condition=waardenburgsyndrome/show/OMIM
ghr.nlm.nih.gov
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Health Information - MMCI
MMCI - Methodist Medical Center, methodist hospital, Illinois hospital, ... Waardenburg syndrome. Waardenburg-Shah syndrome. Wake robin poisoning. Wakefulness ...
http://mmci2.adam.com/content.aspx?productId=101&alpha=W
mmci2.adam.com
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Different colored eyes. Waardenburg syndrome.
... 277-8. Different colored eyes. Waardenburg syndrome. Charrow J. ... Hearing Loss, Sensorineural/etiology. Humans. Infant. Male. Waardenburg's Syndrome/diagnosis ...
http://www.ncbi.nlm.nih.gov/pubmed/17515165
www.ncbi.nlm.nih.gov
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MedlinePlus Medical Encyclopedia: Topics beginning with W
Waardenburg-Shah syndrome see Waardenburg syndrome. Waardenburg syndrome ... Wermer syndrome see Multiple endocrine neoplasia (MEN) I ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_W.htm
www.nlm.nih.gov
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Orphanet: Waardenburg Shah syndrome
The portal for rare diseases ... Waardenburg-Shah syndrome (WSS) is a neurocristopathy ... leukodystrophy, Waardenburg syndrome, and Hirschsprung ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=897
www.orpha.net
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PAX3 - paired box 3 - Genetics Home Reference
Waardenburg syndrome - caused by mutations in the PAX3 gene ... paired box gene 3 (Waardenburg syndrome 1) paired box homeotic gene 3. paired domain gene 3 ...
http://ghr.nlm.nih.gov/gene=pax3
ghr.nlm.nih.gov
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Northside Hospital Medical Referrence Library
Waardenburg syndrome. Waardenburg-Shah syndrome. Wake robin poisoning. Wakefulness ... Wolff-Parkinson-White syndrome. Women and heart disease. Wonderberry poisoning ...
http://northside.adam.com/content.aspx?productId=101&alpha=W
northside.adam.com
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Introduction: Pigmentation Disorders: Merck Manual Professional
Focal hypo- or depigmentation is also a feature of vitiligo (which may involve ... and genetic conditions (tuberous sclerosis, piebaldism, Waardenburg's syndrome) ...
http://www.merck.com/mmpe/print/sec10/ch123/ch123a.html
www.merck.com
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SOX10 - SRY (sex determining region Y)-box 10 - Genetics Home Reference
Waardenburg syndrome - caused by mutations in the SOX10 gene ... This type of Waardenburg syndrome is characterized by changes in skin, hair, and ...
http://ghr.nlm.nih.gov/gene=sox10
ghr.nlm.nih.gov
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When the darker eye has the smaller pupil.
... effects of the concomitant Waardenburg syndrome on the contralateral iris pigmentation. ... Waardenburg's Syndrome/physiopathology. PMID: 12825064 [PubMed ...
http://www.ncbi.nlm.nih.gov/pubmed/12825064
www.ncbi.nlm.nih.gov
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Ministry Health Care
Waardenburg syndrome (Condition) Waardenburg-Shah syndrome (Condition) Wake robin poisoning ... Wernicke-Korsakoff syndrome (Condition) West Nile virus (Condition) ...
http://ministryhealth.adam.com/content.aspx?productId=26&pid=26&alpha=W
ministryhealth.adam.com
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Hearing Loss (Deafness) Information on MedicineNet.com
Hearing loss (deafness) may be present at birth or it may manifest later ... a white forelock, and be caused by a genetic disease called Waardenburg syndrome. ...
http://www.medicinenet.com/guide.asp?s=rss&a=2011&k=Usher_Syndrome_Specialty
www.medicinenet.com
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Waardenburg Syndrome Type I -- GeneReviews -- NCBI Bookshelf
Waardenburg syndrome type I (WS1) is an auditory-pigmentary disorder comprising ... The phenotype of Waardenburg syndrome type I is variable even within a family. ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ws1
www.ncbi.nlm.nih.gov
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Waardenburg syndrome.
... Dermatol Venereol. 2001 Jul;15(4):330-3. Waardenburg syndrome. Konno P, Silm H. ... Waardenburg syndrome (WS) is caused by autosomal dominant mutations, and is ...
http://www.ncbi.nlm.nih.gov/pubmed/11730045
www.ncbi.nlm.nih.gov
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Waardenburg syndrome - Educational resources - Information pages ...
... in the Genetics Home Reference condition summary on Waardenburg syndrome. ... Orphanet: Waardenburg syndrome type 1. Orphanet: Waardenburg syndrome type 2 ...
http://ghr.nlm.nih.gov/condition=waardenburgsyndrome/show/Educational+resources
ghr.nlm.nih.gov
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Albinism
Chediak-Higashi syndrome (lack of coloring all over the skin, but not complete) ... Waardenburg syndrome (often a lock of hair that grows on the forehead, or no ...
http://adam.about.com/encyclopedia/infectiousdiseases/Albinism.htm
adam.about.com
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Craniofacial Abnormalities: Congenital Craniofacial and Musculoskeletal ...
Syndrome. Typical Findings. Waardenburg's syndrome ... Treacher Collins syndrome ... Velocardiofacial syndrome ...
http://merck.com/mmpe/sec19/ch288/ch288d.html
merck.com
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Presbyterian: Healthy Living
Waardenburg syndrome (Condition) Waardenburg-Shah syndrome (Condition) Wake robin poisoning ... Wolff-Parkinson-White syndrome (Condition) Woman's Laxative ...
http://phsorg.adam.com/content.aspx?productId=26&pid=26&alpha=W
phsorg.adam.com
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Waardenburg syndrome.
Type III WS (Klein-Waardenburg syndrome, with abnormalities of the arms) is an ... Type IV WS (Shah-Waardenburg syndrome with Hirschsprung disease) can be caused ...
http://www.ncbi.nlm.nih.gov/pubmed/9279758
www.ncbi.nlm.nih.gov
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Waardenburg syndrome
Genes and Disease provides an introduction to the relationship between genetic factors and human disease with a summary of ~60 genetic diseases with links to related ...
http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=gnd.section.187
www.ncbi.nlm.nih.gov
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EDN3 - endothelin 3 - Genetics Home Reference
Waardenburg syndrome - caused by mutations in the EDN3 gene ... This type of Waardenburg syndrome is characterized by changes in skin, hair, and ...
http://ghr.nlm.nih.gov/gene=edn3
ghr.nlm.nih.gov
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Northside Hospital Medical Referrence Library
Search Results. Waardenburg syndrome. Waardenburg-Shah syndrome. Wake robin poisoning ... Wolff-Parkinson-White syndrome. Women and heart disease. Wonderberry ...
http://northside.adam.com/content.aspx?productId=39&alpha=W
northside.adam.com
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Gilbert Syndrome Glossary of Terms with Definitions on MedicineNet.com
Gilbert Syndrome glossary includes a list of Gilbert Syndrome related medical ... and MSH6 genes for colon cancer , and the PAX3 gene for Waardenburg syndrome. ...
http://www.medicinenet.com/gilbert_syndrome/glossary.htm
www.medicinenet.com
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Waardenburg syndrome associated with meningomyelocele.
1993 Feb 15;45(4):536-7. Waardenburg syndrome associated with meningomyelocele. ... Waardenburg's Syndrome/complications* Waardenburg's Syndrome/genetics ...
http://www.ncbi.nlm.nih.gov/pubmed/1308353
www.ncbi.nlm.nih.gov
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EDNRB - endothelin receptor type B - Genetics Home Reference
Waardenburg syndrome - caused by mutations in the EDNRB gene ... This type of Waardenburg syndrome is characterized by changes in skin, hair, and ...
http://ghr.nlm.nih.gov/gene=ednrb
ghr.nlm.nih.gov
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View Article
... 2004 07 08 2004 08 24 2006 11 15 0017-6192 52 6 2004 Jun [Waardenburg syndrome. ... Incidence Penetrance Phenotype Turkey epidemiology Waardenburg's Syndrome ...
http://www.ncbi.nlm.nih.gov/pubmed/15029423
www.ncbi.nlm.nih.gov
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Waardenburg Syndrome - Yahoo! Health
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 ...
http://health.yahoo.com/children-genetic/waardenburg-syndrom...
health.yahoo.com
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Southwest General Hospital
Waardenburg-Shah syndrome  (Condition) Wake robin poisoning  (Poison) Wakefulness  ... Wolff-Parkinson-White syndrome  (Condition) Women and heart disease ...
http://swgeneralhospital.adam.com/content.aspx?productId=26&pid=26&alpha=W
swgeneralhospital.adam.com
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Ear, nose, and throat - Genetics Home Reference
Angiomatosis retinae see von Hippel-Lindau syndrome ... BDLS see Cornelia de Lange syndrome ... Waardenburg syndrome. Weissenbacher-Zweymüller syndrome ...
http://www.ghr.nlm.nih.gov/ghr/conditionsByCategory/show/earnoseandthroat
www.ghr.nlm.nih.gov
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MITF - microphthalmia-associated transcription factor - Genetics Home ...
Waardenburg syndrome - caused by mutations in the MITF gene ... loss of pigmentation that are characteristic features of Waardenburg syndrome. ...
http://ghr.nlm.nih.gov/gene=mitf
ghr.nlm.nih.gov
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Pallister-Hall syndrome - Wikipedia, the free encyclopedia
Waardenburg syndrome 1 · Developmental dyspraxia · IPEX · Nail-patella syndrome ... Abdallat Davis Farrage syndrome · Ataxia telangiectasia · Incontinentia pigmenti ...
http://en.wikipedia.org/wiki/Pallister-Hall_syndrome
en.wikipedia.org
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148820
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148820
www.ncbi.nlm.nih.gov
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193500
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193500
www.ncbi.nlm.nih.gov
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277580
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277580
www.ncbi.nlm.nih.gov
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Waardenburg syndrome type I
Waardenburg syndrome type I associates at least 2 major or 1 major and ... Waardenburg's syndrome patients have. mutations in the human homologue of the Pax-3 ...
http://www.orpha.net/data/patho/GB/uk-WS1(05).pdf
www.orpha.net
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[Blue eyes on dark background. Waardenburg syndrome]
1: Duodecim. 2005;121(21):2307. [Blue eyes on dark background. Waardenburg syndrome] ... Waardenburg's Syndrome/surgery. PMID: 16457110 [PubMed - indexed for MEDLINE] ...
http://www.ncbi.nlm.nih.gov/pubmed/16457110
www.ncbi.nlm.nih.gov
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