Waardenburg's syndrome

Waardenburg's syndrome
Waar·den·burg's syndrome 'värd-ən-.bərgz- n a highly variable genetic disorder inherited as an autosomal dominant trait and accompanied by all, any, or none of deafness, a white forelock, widely spaced eyes, and heterochromia of the irises
Waar·den·burg 'värd-ən-.bu̇rk Petrus Johannes (1886-1979)
Dutch ophthalmologist. Waardenburg published his description of Waardenburg's syndrome in 1951. The same syndrome had been reported on by J. van der Hoeve in 1916 and D. Klein in 1950.

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an inherited form of deafness accompanied by a characteristic white forelock of hair and multiple colours within the irises of the eyes. It is inherited as an autosomal dominant disease, i.e. the children of an affected parent have a 50% chance of inheriting the disorder, although severity is variable. The gene responsible has been identified.
P. J. Waardenburg (1886-1979), Dutch ophthalmologist

Medical dictionary. 2011.

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  • Waardenburg's syndrome — Autosomal dominant disorder with deafness and pigmentary disturbances probably as a result of defects in function of neural crest. Various forms of the syndrome are recognized. Waardenburg Syndrome 1 (WS1) and WS3 (also known as Klein Waardenburg …   Dictionary of molecular biology

  • Waardenburg-Shah syndrome — Waardenburg s. type 4 …   Medical dictionary

  • Waardenburg-Shah syndrome — Waar·den·burg Shah syndrome (vahrґden boorg shahґ) [P.J. Waardenburg; Krishnakumar N. Shah, Indian physician, late 20th century] Waardenburg syndrome type 4; see under syndrome …   Medical dictionary

  • Waardenburg's syndrome — an inherited form of deafness accompanied by a characteristic white forelock of hair and multiple colours within the irises of the eyes. It is inherited as an autosomal dominant disease, i.e. the children of an affected parent have a 50% chance… …   The new mediacal dictionary

  • Syndrome de waardenburg — Le syndrome de Waardenburg est une maladie génétique de transmission autosomique dominante associant une surdité avec des anomalies de la pigmentation de la peau, des cheveux et/ou de l iris. Le syndrome de Waardenburg est la cause la plus… …   Wikipédia en Français

  • Waardenburg syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 14021 DiseasesDB mult= DiseasesDB2|33475 ICD10 = ICD10|E|70|3|e|70 (ILDS E70.32) ICD9 = ICD9|270.2 ICDO = OMIM = OMIM mult = MedlinePlus = 001428 eMedicineSubj = ped eMedicineTopic = 2422… …   Wikipedia

  • Waardenburg-Shah-Syndrom — Klassifikation nach ICD 10 Q87.8[1] Sonstige näher bezeichnete angeborene Fehlbildungssyndrome, anderenorts nicht klassifiziert …   Deutsch Wikipedia

  • Waardenburg-Syndrom — Klassifikation nach ICD 10 Q87.8[1] Sonstige näher bezeichnete angeborene Fehlbildungssyndrome, anderenorts nicht klassifiziert …   Deutsch Wikipedia

  • Syndrome ABCD — Morphologie faciale du syndrome de Waardenburg Le syndrome ABCD est défini par l association d un albinisme avec une mèche noire, de troubles de la migration des neurocytes de l intestin (maladie de Hirschsprung) et d une surdité neurosensorielle …   Wikipédia en Français

  • Syndrome de Waardenburg — Classification et ressources externes CIM 10 E70.3 (ILDS E70.32) CIM 9 270.2 DiseasesDB …   Wikipédia en Français

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