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Year : 2012  |  Volume : 18  |  Issue : 4  |  Page : 220-222

Waardenburg syndrome 2

Department of Otorhinolaryngology and Head and Neck Surgery, BPS Government Medical College for Women, Sonipat, Haryana, India

Correspondence Address:
Uma Garg
Department of ENT, BPS Government Medical College for Women, Khanpur Kalan, Sonipat, Haryana
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0971-7749.104804

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Waardenburg syndrome (WS) is a rare disease characterised by sensorineural deafness in association with oculocutaneous pigmentary anomalies and dystopia canthorum. In this article, we report a 6-year-old boy with WS2, one of four clinical types of WS, for its rarity and relative paucity of reports in the otological literature. We also review the relevant literature of this rare disorder.

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