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Waardenburg syndrome
(redirected from Waardenburg's syndrome)

   Also found in: Medical, Encyclopedia, Wikipedia 0.01 sec.
Waar·den·burg syndrome  (wôrdn-bûrg, vär-)
n.
A hereditary syndrome characterized by varying degrees of deafness and facial bone defects and by variation in pigmentation of the skin, hair, or eyes.

[After Petrus Johannes Waardenburg (1886-1979), Dutch ophthalmologist.]


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These findings led us to conclude that it is necessary to use otoacoustic emissions in patients with Waardenburg's syndrome in order to provide optimum fitting of hearing aids, especially in children.
In 1992, for example, investigators found the mutated gene behind Waardenburg's syndrome, a condition characterized by deafness, widely spaced eyes that are sometimes mismatched in color, and a white forelock (SN: 5/2/92, p.
Waardenburg's syndrome arises when certain pigment-forming cells in the embryo fail to migrate from the neural crest to the eyes, hair, skin, or ears.
 
 
 
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