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...

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

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

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

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

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...

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

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