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

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...

considered a separate syndrome, ABCD syndrome is today considered to be a variation of Shah-Waardenburg type IV. Waardenburg syndrome (WS) is described as...

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

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...

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

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

in the application of genetics to ophthalmology. Waardenburg syndrome is named after him. Waardenburg studied medicine at the Utrecht University from 1904–11...

in a "leucistic" appearance include piebaldism, Waardenburg syndrome, vitiligo, Chédiak–Higashi syndrome, flavism, isabellinism, xanthochromism, axanthism...

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