Home Ahead of print Instructions Contacts
About us Current issue Submit article Advertise  
Editorial board Archives Subscribe Login   
CASE REPORT
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
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-7749.104804

Rights and Permissions

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.


[FULL TEXT] [PDF]*
Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed2390    
    Printed84    
    Emailed0    
    PDF Downloaded266    
    Comments [Add]    

Recommend this journal