Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies...

Waardenburg is a village in the Dutch province of Gelderland. It is a part of the municipality of West Betuwe, and is located about 13 km west of Tiel...

Waardenburg syndrome type 1 is a congenital disorder that caused by a mutation in the PAX3 gene that results in abnormal development in the neural crest...

Waardenburg is a town in the municipality of Neerijnen, province of Gelderland, Netherlands. The Dutch name Waardenburg may also refer to: Waardenburg...

Waardenburg syndrome type 4A is an extremely rare congenital disorder caused by a mutation in an endothelin receptor gene. It results in common Waardenburg...

Lucien Joseph van Waardenburg (21 February 1900 – 4 April 1975) was the first Dutch-appointed governor of Dutch New Guinea. Van Waardenburg was born in Buitenzorg...

Waardenburg syndrome type 2D, a subtype of the Waardenburg syndrome, is a rare congenital disorder caused by a mutation in the SLUG (SNAI2) gene. It is...

Waardenburg Castle, sometimes also called Weerdenburg, is a medieval castle located in Waardenburg in the municipality of West Betuwe, in the Dutch province...

gene, which affects the migration of melanoblasts during development. Waardenburg Syndrome: This neural crest disorder is associated with sensorineural...

Waardenburg anophthalmia syndrome is a rare autosomal recessive genetic disorder which is characterized by either microphthalmia or anophthalmia, osseous...

Horner's syndrome – sometimes inherited, although usually acquired. Waardenburg syndrome – a syndrome in which heterochromia is expressed as a bilateral...

Waaler–Aarskog syndrome Waardenburg anophthalmia syndrome Waardenburg syndrome Waardenburg syndrome type 1 Waardenburg syndrome type 2 Waardenburg syndrome type...

head, have a congenital deafness (partial or total) which is similar to Waardenburg syndrome in humans. Ferrets without white markings, but with premature...

variety of complications including Waardenburg syndrome I and III as well as craniofacial-deafness-hand syndrome. Waardenburg syndrome is most often associated...

giving an appearance of a widened nasal bridge. It is associated with Waardenburg syndrome, which is due to mutation in PAX gene. Anatomy portal Animals...

neurocristopathies, which include conditions such as frontonasal dysplasia, Waardenburg–Shah syndrome, and DiGeorge syndrome. Defining the mechanisms of neural...

apart than most people's. This is due to a genetic condition known as Waardenburg syndrome. The condition has also left Sanjati deaf in her left ear. In...

Petrus Johannes Waardenburg (1886–1979) brought about the idea of Waardenburg syndrome when he examined two deaf twins. Waardenburg decided to define...

conditions that result in a "leucistic" appearance include piebaldism, Waardenburg syndrome, vitiligo, Chédiak–Higashi syndrome, flavism, isabellinism,...

syndrome, Klinefelter syndrome, Turner syndrome, Ehlers–Danlos syndrome, Waardenburg syndrome often present with prominent epicanthal folds, and if these...

Petrus Johannes Waardenburg (3 June 1886 – 23 September 1979) was a Dutch ophthalmologist, geneticist, and pioneer in the application of genetics to ophthalmology...

the inner canthi of the eyes. Dystopia canthorum is associated with Waardenburg syndrome. Aquiline nose – Human nose with a prominent bridge Bridge piercing –...

piebaldism occurs together with severe developmental problems, as in Waardenburg syndrome and Hirschsprung's disease. Piebaldism has been documented to...

gene also has clinical significance, being linked to diseases such as Waardenburg Syndrome and rhabdomyosarcoma. The gooseberry gene was first described...

Dokter Faust van Waardenburg is a protagonist from a folk tale that is famous in the Netherlands. It is a Dutch version of the German Faust tale. The...

Community: Members’ Choice MVP: Coaches Award: 2024–25 NBL season "Sam Waardenburg signs extension with Cairns Taipans". ESPN.com.au. 30 January 2024. Retrieved...

studies have been done to link this to genes known to be involved in human Waardenburg syndrome, a syndrome of hearing loss and depigmentation caused by a genetic...

2008, p. 280. De Young 2004, p. 60. Riddell 2001, p. 235. Waardenburg 1999, p. 276. Waardenburg 1999, p. 255. De Young 2004, p. 64. Anthony 2011, p. 68...

is not to be confused with Wartenberg's migratory sensory neuropathy, Waardenburg syndrome, or Lateral medullary syndrome (known as Wallenberg's Syndrome)...

Without this fluid, the eye fails to enlarge, resulting in microphthalmia. Waardenburg syndrome type 2 in humans may also be caused by mutations in MITF The...