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Waardenburg Syndrome Type I: An Otorhinolaryngologist's Perspective | OMICS International| Abstract
ISSN: 2161-119X

Otolaryngology: Open Access
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  • Case Report   
  • Otolaryngol (Sunnyvale),
  • DOI: 10.4172/2161-119X.1000383

Waardenburg Syndrome Type I: An Otorhinolaryngologist's Perspective

Abhilasha Goswami* and Kalpana Sharma
Department of Otorhinolaryngology, Gauhati Medical College, Assam, India
*Corresponding Author : Abhilasha Goswami MBBS, Post-graduate trainee, Department of Otorhinolaryngology, Gauhati Medical College, Assam, India, Tel: +918638866493, Email: [email protected]

Received Date: Sep 08, 2019 / Accepted Date: Oct 31, 2019 / Published Date: Nov 07, 2019

Abstract

Waardenburg syndrome type I is a rare, autosomal dominant auditory-pigmentary syndrome characterized by congenital sensorineural hearing loss, pigmentary abnormalities of the iris, hair and skin, and dystopia canthorum. Waardenburg syndrome affects an estimated 1 in 40,000 people. It accounts for 2 to 5 percent of all cases of congenital hearing loss. Here, we present the case of an 11-month old girl with Waardenburg syndrome type I.

Keywords: Waardenburg syndrome type I; Sensorineural hearing loss; Blue iris; Dystopia canthorum

Citation: Goswami A, Sharma K (2019) Waardenburg Syndrome Type I: An Otorhinolaryngologist’s Perspective. Otolaryngol (Sunnyvale) 9: 383. Doi: 10.4172/2161-119X.1000383

Copyright: © 2019 Goswami A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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