Waardenburg Syndrome


Klein Syndrome

Klein Waardenburg Syndrome

Klein's Syndrome

Klein-Waardenburg Syndrome

Kleins Syndrome

Syndrome, Klein

Syndrome, Klein's

Syndrome, Klein-Waardenburg

Syndrome, Waardenburg

Syndrome, Waardenburg's

Syndrome, Waardenburg-Klein

Waardenburg Klein Syndrome

Waardenburg Syndrome Type 1

Waardenburg Syndrome Type 3

Waardenburg Syndrome with Dystopia Canthorum

Waardenburg Syndrome with Upper Limb Anomalies

Waardenburg Syndrome, Type 1

Waardenburg Syndrome, Type 3

Waardenburg Syndrome, Type III

Waardenburg's Syndrome

Waardenburg's Syndrome Type 1

Waardenburg-Klein Syndrome

Waardenburgs Syndrome

White Forelock (Poliosis) Syndrome with Multiple Congenital Malformations

Rare, autosomal dominant disease with variable penetrance and several known clinical types. Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities.

See Also