Conditions / Syndrome
Waardenburg syndrome type 2B
info · Syndrome
A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome reg
A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome region 1p21-p13.3.
Signs and symptoms
- Heterochromia iridis
- White forelock
- Sensorineural hearing impairment
- Premature graying of hair
- Telecanthus
- Abnormal facial shape
Also known as: WS2B; Waardenburg syndrome type IIB