Waardenburg syndrome is usually inherited as an autosomal dominant trait, meaning only one parent has to pass on the faulty gene for a child to be affected.
There are four main types of Waardenburg syndrome. The most common are type I and type II.
Type III (Klein-Waardenburg syndrome) and type IV (Waardenburg-Shah syndrome) are more rare.
The multiple types of this syndrome result from defects in different genes. Most people with this disease have a parent with the disease, but the symptoms in the parent can be quite different from those in the child.
Symptoms may include:
Cleft lip (rare)
Deafness (more common in type II disease)
Extremely pale blue eyes or eye colors that don't match (heterochromia)
Pale color skin, hair, and eyes (partial albinism)
Difficulty completely straightening joints
Possible slight decrease in intellectual function
Wide-set eyes (in type I)
White patch of hair or early graying of the hair
Less common types of this disease may cause problems with the arms or intestines.
There is no specific treatment. Symptoms will be treated as appropriate. Special diets and medicines to keep the bowel moving are prescribed to those patients who have constipation. Hearing should be monitored closely.
Once hearing problems are corrected, most people with this syndrome should be able to lead a normal life. Those with rarer forms of the syndrome may have other complications.
Constipation severe enough to require part of large bowel to be removed
Self-esteem problems, or other problems related to appearance
Slight increased risk for muscle tumor called rhabdomyosarcoma
When to Contact a Medical Professional
Genetic counseling may be helpful if you have a family history of Waardenburg syndrome and plan to have children. Call for a hearing test if you or your child has deafness or decreased hearing.
Milunsky JM. Waardenburg Syndrome Type I. 2001 Jul 30 [Updated 2011 Dec 29]. In: Pagon RA, Adam MP, Bird TD, et al., editors. GeneReviews™ [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2013.
Chad Haldeman-Englert, MD, FACMG, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Bethanne Black, and the A.D.A.M. Editorial team.