Waardenburg Syndrome

Waardenburg syndrome is a genetic condition that combines changes in the pigmentation of the skin, hair and eyes with varying degrees of hearing loss present from birth. It is inherited and can present in different ways within the same family.

Common features: a white lock of hair, eyes of different colors or very light-colored, greater spacing between the eyes and decreased hearing.

When to get checked? with signs of low hearing in a baby or child, especially if accompanied by striking pigmentation features or a family history.

Which specialist treats it? the otolaryngologist is in charge of evaluating hearing and the pediatrician supports overall development. Having it assessed in a timely manner by a professional makes it easier to provide the follow-up and support needed.