Cellosaurus Disease Terminology Syndrome Rare Non-Neoplastic Disorder Waardenburg Syndrome Waardenburg's Syndrome Cellosaurus C3266898 A rare, autosomal dominant inherited syndrome caused by mutations in the PAX3, MITF, and SNAI2 genes. Signs and symptoms include hearing loss, dystopia canthorum (widely spaced inner corners of the eyes), and changes in the color of the skin, hair, and eyes. Waardenburg Syndrome Waardenburg Syndrome NICHD Disease or Syndrome C85222 NICHD Terminology Neonatal Research Network Terminology