41. MyDNA.com - Waardenburg Syndrome myDNA is a consumer focused health, genetics, and genomics information provider offering disease condition information, health wellness tips, http://www.mydna.com/genes/genetics/disorders/disease/neonatal/ws.html

@import url(http://www.mydna.com/plone.css); @import url(http://www.mydna.com/ploneCustom.css); myDNA.com Search Yellow Pages News ... Diets Search For In Entire Site Articles News Images Advanced Search Home Genetics Center ... Neonatal Diseases Waardenburg Syndrome Page Tools Print This Page E-Mail This Page Add to Favorites Genetics Genetics News Ask Dr. DNA Top Tens Genetics 101 Genetic Testing Genetic Disorders Genes and Disease Blood Diseases Cancer Digestive System Ear, Nose and Throat Female-Specific Disease Glands and Hormones Heart and Blood Vessels Immune System Male Specific Disease Muscle and Bone Neonatal Diseases Nervous System Nutritional and Metabolic Respiratory Diseases Skin, Connective Tissue

42. Waardenburg Syndrome waardenburg syndrome like any disease comes about as a malfunction of one or waardenburg syndrome (WS) is an inherited disorder often characterized by http://www.tjclarkinc.com/d_waardenburg_syndrome.htm

Deutsche Version USRMA Health Search Wizard 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. Does what you eat provide all the essential elements you need? See Senate Document 264. Just how good is the "best" diet? See The Food Pyramid Waardenburg Syndrome 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.

43. Waardenburg's Syndrome This brief publicorientated fact sheet about waardenburg syndrome is made available on the Web by the National Institute on Deafness and other http://omni.ac.uk/browse/mesh/D014849.html

low graphics Waardenburg's Syndrome broader: Abnormalities, Multiple other: Alagille Syndrome Angelman Syndrome Beckwith-Wiedemann Syndrome Branchio-Oto-Renal Syndrome ... Waardenburg syndrome This brief public-orientated fact sheet about Waardenburg Syndrome is made available on the Web by the National Institute on Deafness and other Communication Disorders, which is part of the US National Institutes of Health. The leaflet explains what this condition is, the different types of Waardenburg Syndrome, and the causes of the condition. Waardenburg's Syndrome Patient Education Handout [Publication Type] Last modified: 09 Sep 2005

44. Waardenburg Syndrome waardenburg syndrome is a genetic disorder that may be evident at birth (congenital). The range and severity of associated symptoms and findings may vary http://www.bchealthguide.org/kbase/nord/nord430.htm

var hwPrint=1;var hwDocHWID="nord430";var hwDocTitle="Waardenburg Syndrome";var hwRank="1";var hwSectionHWID="nord430-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. 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

45. Waardenburg Syndrome - Definition From Biology-Online.org Definition and other additional information on waardenburg syndrome from BiologyOnline.org dictionary. http://www.biology-online.org/dictionary/waardenburg_syndrome

Forum Tutorials Dictionary Directory ... W waardenburg syndrome Waardenburg syndrome (Science: syndrome) Rare autosomal dominant disease with variable penetrance and several known clinical types Clinical features include depigmentation of the skin and hair with a white forelock congenital cochlear deafness ... heterochromia iridis or hypochromia iridis, medial eyebrow hyperplasia hypertrophy of the nasal root producing increased width of the root of the nose dystopia canthorum, lateral dystopia of medial canthi and lacrimal puncta and synophrys The underlying cause may be defective development of the neural crest neurocristopathy Waardenburg's syndrome may be closely related to piebaldism . Klein- waardenburg syndrome refers to a disorder that also includes upper limb abnormalities Inheritance : audosomal dominant Search the dictionary About Us Contact Us Link to Us Chemistry ... Equations

46. Waardenburg Syndrome waardenburg syndrome, Search. waardenburg syndrome. waardenburg syndrome is an autosomal dominant hereditary condition. It is characterized mainly by http://www.drhull.com/EncyMaster/W/Waardenburg_syndrome.html

Help for sleepless parents 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.

47. Waardenburg Syndrome - Definition Of Waardenburg Syndrome By The Free Online Dic Definition of waardenburg syndrome in the Online Dictionary. Meaning of waardenburg syndrome. What does waardenburg syndrome mean? waardenburg syndrome http://www.thefreedictionary.com/Waardenburg syndrome

Domain='thefreedictionary.com' word='Waardenburg syndrome' Your help is needed: American Red Cross The Salvation Army join mailing list webmaster tools Word (phrase): Word Starts with Ends with Definition subscription: Dictionary/ thesaurus Computing dictionary Medical dictionary Legal dictionary Financial dictionary Acronyms Columbia encyclopedia Wikipedia encyclopedia Hutchinson encyclopedia Waardenburg syndrome Also found in: Medical Wikipedia 0.02 sec. Page tools Printer friendly Cite / link Email Feedback Waar·den·burg syndrome (wôr dn-bûrg , vär n. A hereditary syndrome characterized by varying degrees of deafness and facial bone defects and by variation in pigmentation of the skin, hair, or eyes. [After Petrus Johannes Waardenburg (1886-1979), Dutch ophthalmologist.] Mentioned in References in classic literature No references found No references found Dictionary/thesaurus browser Full browser Wa'n't wa-wa WAAC WAAF ... Waal Waardenburg syndrome Wabanaki Wabash Wabash River wabble ... WAAR Waardenburg syndrome Waardenburg's syndrome Waardenburg's syndrome Waaree Instrument Calibration Laboratory Waarnemend ... Waart, Edo de

48. Hill Health Topics A-Z - Waardenburg Syndrome waardenburg syndrome. National Organization for Rare Disorders. Important It is possible that the main title of the report waardenburg syndrome is not the http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord430&SE

49. Waardenburg Syndrome Anatomic variations of the medial canthus in waardenburg syndrome. , Mother and 5-year-old son with waardenburg syndrome type 1. http://www.medlink.com/PublicCIP.ASP?access=public&UID=MLT002G1&code=

50. Waardenburg's Syndrome Topic - Unified Search Environment MSH/PM/D014849 MSH/PM/D014849 CSP/PT/40060098 MTHICD9/ET/270.2 MSH/PM/D014849 van der Hoeve Halbertsona waardenburg syndrome CSP/SY/4006-0098 http://www.use.hcn.com.au/portals/shared/subject.`Waardenburg's Syndrome`/home.h

Waardenburg's Syndrome Topic Tree Definition: name used for several different hereditary syndromes, see UFs for specifics. Synonyms and Source Vocabularies: Waardenburg's Syndrome van der Hoeve Halbertsona Waardenburg syndrome Congenital Abnormality Abnormalities, Drug-Induced Abnormalities, Multiple Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome Bloom Syndrome Cockayne Syndrome ... Congenital neurologic anomalies

51. BBC - H2g2 - Waardenburg Syndrome h2g2 is the unconventional guide to life, the universe and everything, a guide that s written by visitors to the website, creating an organic and evolving http://www.bbc.co.uk/dna/h2g2/A677991

@import url('/includes/tbenh.css') ; Home TV Radio Talk ... A-Z Index Friday 9th September 2005 Text only Guide ID: A677991 (Edited) Edited Guide Entry SEARCH h2g2 Advanced Search New visitors: Returning members: BBC Homepage The Guide to Life The Universe and Everything 1. Life Created: 31st January 2002 Waardenburg Syndrome Front Page What is h2g2? Who's Online Write an Entry ... Help Like this page? Send it to a friend! Waardenburg Syndrome (WS) is not as severe as other genetic disorders, as its effects are physical as opposed to mental, but it can still affect the daily life of the afflicted. It was named after the Dutch eye doctor Petrus Johannes Waardenburg who noticed that his patients with differently coloured eyes (heterochromia) also suffered from hearing loss. He then went on to study over 1000 patients with a history of hearing loss in their family and found several physical traits that were shared. Types of the Disorder There are at least four types of WS, the most common named Type One and Type Two. The different types are defined by the distinct physical traits of those beset with the syndrome. Patients with Type One have an unusually wide space between the corners of their eyes. 20% of individuals with Type One experience hearing loss. Those with normal eye spacing but many other WS traits have Type Two. About half of these patients have hearing impairments. Some Symptoms The symptoms of WS include a blaze of white or grey in otherwise normally coloured hair, abnormally spaced eyes, one brown and one blue eye or brilliantly blue eyes. Connected eyebrows, a broad nose and a low frontal hairline are also common phenotypes of WS. An afflicted individual may have all of these symptoms or only a few.

52. Waardenburg Syndrome 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

53. Waardenburg Syndrome - Talk Medical Humanfriendly medical definition of waardenburg syndrome. http://www.talkmedical.com/medical-dictionary/15368/Waardenburg-Syndrome

Home Medications Medical Dictionary Talk Medical ... Medical Dictionary Newsletter Subscribe to the free monthly health digest. Relevant health articles just for you. Tell a friend Waardenburg Syndrome Waardenburg syndrome: A genetic disorder that causes deafness, white forelock (a frontal white blaze of hair), a difference of color between the iris of one eye and the other (heterochromia iridis), white eye lashes, and wide-set inner corners of the eyes. The deafness is typically congenital (present at birth), bilateral, profound sensorineural (nerve) deafness. The severity of Waardenburg syndrome (WS) varies and about 40 percent of affected persons escape the deafness. The white forelock may be present at birth. The majority of individuals with WS have the white forelock or early graying of the scalp hair before age 30. WS is inherited in an autosomal dominant manner in which the heterozygous state (with one copy of the gene) is sufficient to cause the syndrome. The homozygous form of WS with two copies of the gene is a very severe (and fortunately rare) disorder with very severe upper-limb defects that has been called the Klein-Waardenburg syndrome. The gene for classic WS, symbolized WS1, is on chromosome 2 (in band q35) and is the PAX3 gene which encodes a DNA-binding transcription factor that is expressed in the early embryo. The syndrome is named for a Dutch eye doctor named Petrus Johannes Waardenburg (1886-1979) who first noticed that people with differently colored eyes often had a hearing impairment.

54. Waardenburg Syndrome Type 3 Information Diseases Database waardenburg syndrome type 3,Kleinwaardenburg syndrome, Disease Database Information. http://www.diseasesdatabase.com/ddb33475.htm

Diseases Database Index Sponsors Contact ... Previous Page Waardenburg syndrome type 3 information Search 2 synonyms or equivalents were found. Waardenburg syndrome type 3 aka/or Klein-Waardenburg syndrome may cause or feature (Follow link for list.) may be allelic with (Follow link for list.) belong(s) to the category of (Follow link for list.) Waardenburg syndrome type 3: Definition(s) via UMLS Code translations and terms via UMLS Waardenburg syndrome type 3: specific web sites Send Waardenburg syndrome type 3 to medical search engines (JavaScript enabled browsers only.) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation Valid XHTML 1.0 Served 2005-09-09 22:06:53 View metadata Last major update 2005-09-03. The medical information here is presented for education, background reading and general interest. The Diseases Database is not a diagnostic or clinical decision-making tool. Please consult your own licensed physician regarding diagnosis and treatment of any medical condition!

55. Pamphlet By: National Institute On Deafness And Other Communication Disorders: W Full text of the article, waardenburg syndrome from Pamphlet by National Institute on Deafness and Other Communication Disorders, a publication in the http://www.findarticles.com/p/articles/mi_m0DVD/is_1999_March/ai_63040378

@import url(/css/us/style1.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); @import url(/css/us/artHome1.css); Advanced Search Home Help IN free articles only all articles this publication Automotive Sports 10,000,000 articles - not found on any other search engine. FindArticles Pamphlet by: National Institute on Deafness and Other Communication Disorders March 1999 Content provided in partnership with 10,000,000 articles Not found on any other search engine. Featured Titles for AAACN Viewpoint ABNF Journal, The AIDS Treatment News AMAA Journal ... View all titles in this topic Hot New Articles by Topic Automotive Sports Top Articles Ever by Topic Automotive Sports Waardenburg Syndrome Pamphlet by: National Institute on Deafness and Other Communication Disorders March, 1999 Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. * Description * Types of WS * Cause * Research studies * Additional online resources 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. Continue article Advertisement 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.

56. Health Management Technology: Waardenburg Syndrome - Industry Trend Or Event Full text of the article, waardenburg syndrome Industry Trend or Event from Health Management Technology, a publication in the field of Health Fitness http://www.findarticles.com/p/articles/mi_m0DUD/is_1999_March/ai_62347959

@import url(/css/us/style1.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); @import url(/css/us/artHome1.css); Advanced Search Home Help IN free articles only all articles this publication Automotive Sports 10,000,000 articles - not found on any other search engine. FindArticles Health Management Technology March 1999 Content provided in partnership with 10,000,000 articles Not found on any other search engine. Related Searches Klein-Waardenburg syndrome / Research Health care industry / Research Featured Titles for AAACN Viewpoint ABNF Journal, The AIDS Treatment News AMAA Journal ... View all titles in this topic Hot New Articles by Topic Automotive Sports Top Articles Ever by Topic Automotive Sports Waardenburg Syndrome - Industry Trend or Event Health Management Technology March, 1999 Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. * Description * Types of WS * Cause * Research studies * Additional online resources 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. Continue article Advertisement 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.

57. Free Online ICD9/ICD9CM Codes And Medical Dictionary Waardenburg s syndrome may be closely related to piebaldism. Kleinwaardenburg syndrome refers to a disorder that also includes upper limb abnormalities. http://icd9cm.chrisendres.com/index.php?action=dictdtl&recordid=12875

58. WAARDENBURG SYNDROME Waardenburg’s Syndrome (WS) is a rare autosomal dominant syndrome Transcription factor hierarchy in waardenburg syndrome regulation of MITF expression http://www.med.wayne.edu/dermatology/MichDerm Online 2002/31WAARDENBURG SYNDROME

CASE 31—WAARDENBURG’S SYNDROME Waardenburg’s 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.

59. Waardenburg Syndrome,WS,Waardenburg Syndrome Type I (WS1 waardenburg syndrome,WS,waardenburg syndrome Type I (WS1),waardenburg syndrome Type II (WS2),waardenburg syndrome Type IIA (WS2A),waardenburg syndrome Type http://www.icomm.ca/geneinfo/waarden.htm

60. Waardenburg Syndrome waardenburg syndrome. NORD waardenburg syndrome Syndromic Hearing Loss waardenburg syndrome waardenburg syndromes. Back to The Cannylink home page http://www.cannylink.com/diseasewaardenburgsyndrome.htm

Web www.CannyLink.com Waardenburg Syndrome NORD - Waardenburg Syndrome Syndromic Hearing Loss Waardenburg Syndrome Waardenburg Syndromes Back to The Cannylink home page You can e-mail us at Webmaster@cannylink

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