Waardenburg syndrome

From WikiMD

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.


WikiMD Resources - Waardenburg syndrome

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Link to this page: <a href="http://www.wikimd.org/wiki/Waardenburg_syndrome">Waardenburg syndrome</a>

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