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Waardenburg Syndrome:     more detail

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

lists with details

41. Swiss-Prot Keyword: Waardenburg Syndrome
    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 IIB  
    http://www.expasy.org/cgi-bin/get-entries?KW=Waardenburg syndrome

42. CMGS-Identification Of The Gene For Waardenburg Syndrome /11.2.99
    Identification of the gene responsible for waardenburg syndrome (WS). Phenotype. Read AP, Foy C, Newton V Exclusion mapping in waardenburg syndrome.  
    http://www.ich.ucl.ac.uk/cmgs/wardsyn.htm
    
    Extractions: Simpson et al. (1974) and Arias et al. (1975) suggested linkage to the ABO locus at 9q34. This was later excluded by Read et al. (1989) and da-Silva et al. (1990). Read et al. (1989) used polymorphic markers to study human chromosome 12, close to PEPB. PEPB is the human homolog of the mouse Pep-2 locus, mutation of which results in the 'Steel' mouse model of WS1. Read et al. (1989) excluded a large part of 12q as the site of the WS gene. Cytogenetic observations indicated which chromosomal areas to investigate.

43. Waardenburg Syndrome Type II
    waardenburg syndrome type II. References Tassabehji M, Newton VE, Read A. waardenburg syndrome type 2 caused by mutations in human microphthalmia (MITF) gene.  
    http://www.orpha.net/data/patho/GB/uk-WS2.html

44. WAARDENBURG SYNDROME : Contact A Family - For Families With Disabled Children: I
    printer friendly, waardenburg syndrome, waardenburg syndrome (WS) is an inherited condition which may be associated with a range of features.  
    http://www.cafamily.org.uk/Direct/w10.html
    
    Extractions: helpful? yes no Waardenburg syndrome (WS) is an inherited condition which may be associated with a range of features. The main characteristics of WS include hearing impairment (see Deafness Gut Motility Disorders ) or features including upper limb abnormalities and cleft lip and/or palate . Individuals with WS have a normal lifespan. Researchers have described four main types of WS. A diagnosis of the particular type of WS depends upon detecting the fault in the causative gene. The different types of WS vary in the physical characteristics present. The most common types of WS are Type 1 and Type 2, which are distinguished on the basis of widely spaced eyes. This feature is present in Type 1 and absent in Type 2. However, hearing impairments are more common in Type 2. Type 3 (Klein-Waardenburg syndrome) is rare and is associated with upper limb abnormalities. Type 4 (Waardenburg-Hirschsprung disease), which is also uncommon, is associated with associated with colon problems originating from the time of birth. Inheritance patterns A number of genes have been associated with WS and different genes are associated with the different types of WS. In most cases, WS is inherited as an autosomal dominant trait. The genetics of Waardenburg-Hirschsprung disease is slightly different as this type of WS is inherited as an autosomal recessive trait.

45. Waardenburg Syndrome And Deafness
    waardenburg syndrome and deafness. I am pregnant with another child whose father s family has a history of waardenburg syndrome and most of them are deaf.  
    http://interact.pregnancytoday.com/cgi-bin/boards/genetic.pl?read=63

46. Re Waardenburg Syndrome And Deafness
    Genetic Issues Discussion Board. Re waardenburg syndrome and deafness. In Response To waardenburg syndrome and deafness (Angel). Angel,. Check out my webpage  
    http://interact.pregnancytoday.com/cgi-bin/boards/genetic.pl?read=67

47. Conditions And Diseases - Waardenburg Syndrome Top Links
    waardenburg syndrome Web Site Links. NORD waardenburg syndrome - A general discussion about this disorder, followed by further resources.  
    http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso

48. Genetic Disorders: Waardenburg Syndrome
    Genetic Disorders waardenburg syndrome. An article about waardenburg syndrome and its features, statistics and the gene pax3. National Library of Medicine.  
    http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/Wa
    
    Extractions: Home Health Conditions and Diseases Genetic Disorders : Waardenburg Syndrome google_ad_client = 'pub-3272565765518472';google_ad_width = 336;google_ad_height = 280;google_ad_format = '336x280_as';google_color_border = 'FFFFFF';google_color_bg = 'FFFFFF';google_ad_channel ='7485447737';google_alternate_color = 'FFFFFF';google_color_link = '0000FF';google_color_url = '008000';google_color_text = '000000';

49. Disease - Waardenburg Syndrome - Hartford, Connecticut , Saint Francis Care
    Disease waardenburg syndrome - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart  
    http://www.saintfranciscare.com/14273.cfm
    
    Extractions: Sense of hearing Definition: Waardenburg syndrome is a group of hereditary conditions characterized by deafness and partial albinism (pale skin, hair and eye color). Causes And Risk: 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 different colored eyes . Affected individuals may also have wide separation of the inner corners of the eyes, a broad nasal bridge, and other color changes of the skin. Waardenburg syndrome affects about 1 in every 30,000 people. Almost 90% of patients have an affected parent but the symptoms in the parent can be quite different from those in the child.

50. Health Library -
    waardenburg syndrome. Important It is possible that the main title of the report waardenburg syndrome is not the name you expected.  
    http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

51. Health Library -
    waardenburg syndrome. Synonyms General Discussion. waardenburg syndrome is a genetic disorder that may be evident at birth (congenital). The  
    http://12.42.224.152/Library/HealthGuide/IllnessConditions/topic.asp?hwid=nord43

52. Waardenburg Syndrome - Deafness And Communication Disorder Terms And Definitions
    Definition for waardenburg syndrome and other Deafness and Communication Disorder Terms by Health Dictionary. waardenburg syndrome  
    http://www.health-dictionary.com/deafness_term_details/Waardenburg_Syndrome
    
    Extractions: document.write(lday + ", " +lmonth + " " + date + ", " + year ) 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. A B C ... W Information and definitions of the medical conditions and diseases have been taken from various reliable government publications and we have done our best to verify their accuracy. If you feel any of the definitions are incorrect or needs to be updated please contact us and we will look into it. Contact Health Dictionary - Medical and Disease Terms and Definitions

53. Health, Conditions And Diseases, Genetic Disorders: Waardenburg Syndrome
    The waardenburg syndrome (WS) gene affects the body in three primary ways hearing , pigmentation (coloring) of the skin, hair and eyes, and facial structure.  
    http://www.combose.com/Health/Conditions_and_Diseases/Genetic_Disorders/Waardenb
    
    Extractions: Related links of interest: The Waardenburg syndrome (WS) gene affects the body in three primary ways: hearing , pigmentation (coloring) of the skin, hair and eyes, and facial structure. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the Open Directory and has been modified and enhanced using our own technology. About ComboSE Download Combose Toolbar

54. PillSupplier.com - Conditions And Diseases/Genetic Disorders/Waardenburg Syndrom
    Category waardenburg syndrome. HOME ABOUT Search Login . Conditions and Diseases/Genetic Disorders/waardenburg syndrome. Links  
    http://www.pillsupplier.com/dir/867/

55. Waardenburg Syndrome With Anisocoria And Exotropia. Dastur YK, Dudhani A, Chital
    waardenburg syndrome with anisocoria and exotropia. Abstract. A case of waardenburg syndrome with unusual features such as anisocoria, exotropia is reported.  
    http://www.jpgmonline.com/article.asp?issn=0022-3859;year=1995;volume=41;issue=4

56. ThirdAge - Adam - Waardenburg Syndrome
    waardenburg syndrome. waardenburg syndrome is inherited as an autosomal dominant trait; only one parent has to pass on the gene for a child to be affected.  
    http://www.thirdage.com/health/adam/ency/article/001428.htm
    
    Extractions: Causes, incidence, and risk factors: 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 different colored eyes heterochromia ). Other findings that may be seen include wide separation of the inner corners of the eyes with a broad nasal bridge and other pigmentary changes of the skin. Waardenburg syndrome affects about 1 in 30,000 people. Almost 90% of patients have an affected parent but the manifestations of the condition in the parent can be quite different from those in the child.

57. :: Ez2Find :: Waardenburg Syndrome
    Guide waardenburg syndrome, Global Metasearch Any Language Guides, waardenburg syndrome. ez2Find Home Directory Health Conditions  
    http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
    
    Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Waardenburg Syndrome Web Sites Human Gene Map [Site Info] [Translate] [Open New Window] National Library of Medicine [Site Info] [Translate] [Open New Window] NORD: Waardenburg Syndrome [Site Info] [Translate] [Open New Window] A general discussion about this disorder, followed by further resources.

58. Waardenburg Syndrome
    The New Health Directory, Directory, Home Health Conditions and Diseases Genetic Disorders waardenburg syndrome (4) See Also  
    http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/Wa

59. Klein Waardenburg Syndrome : On Medical Dictionary Online
    Klein waardenburg syndrome defined on the Free Online Medical Dictionary. Link to the Medical Dictionary Online. Klein waardenburg syndrome.  
    http://www.online-medical-dictionary.org/?q=Klein Waardenburg Syndrome

60. Waardenburg Syndrome : On Medical Dictionary Online
    waardenburg syndrome defined on the Free Online Medical Dictionary. Medical Link to the Medical Dictionary Online. waardenburg syndrome. Rare  
    http://www.online-medical-dictionary.org/?q=Waardenburg Syndrome

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