Waardenburg syndrome type 3

Waardenburg syndrome type 3 (WS3) is a very rare subtype of Waardenburg syndrome (WS) that is characterized by limb anomalies in association with congenital hearing loss, minor defects in structures arising from neural crest, resulting in pigmentation anomalies of eyes, hair, and skin.

Also known as: Klein-Waardenburg syndrome, WS3, Waardenburg syndrome type III, Waardenburg syndrome with limb anomalies, Waardenburg syndrome with upper limb anomalies, Waardenburg syndrome, type 3, White forelock (poliosis) syndrome with multiple congenital malformations

0 clinical trials for this condition and its sub-types, 0 tagged with Waardenburg syndrome type 3 itself.