Waardenburg syndrome type 2

Genetics

• autosomal dominant
• genetically heterogenous

Clinical manifestations

• sensorineural deafness
• pigmentary disturbances
• absence of dystopia canthorum
• frequency of deafness is higher then in Waardenburg's syndrome type 1

More general terms

• Waardenburg syndrome

More specific terms

• Waardenburg syndrome type 2 OA; Waardenburg syndrome type 2 with ocular albinism; WS2-OA
• Waardenburg syndrome type 2A
• Waardenburg syndrome type 2B
• Waardenburg syndrome type 2D
• Waardenburg syndrome type 2E

Database

• OMIM: https://mirror.omim.org/entry/608890