Waardenburg Syndrome

Waardenburg syndrome is a rare genetic disorder characterized by varying degree of deafness associated with pigmentary anomally and defects of neural crest cell derived structures. Four distinct subtypes showing marked interfamilial and intrafamilial variability have been described. We report a girl...

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Bibliographic Details
Main Authors: Yuvika Bansal, Parul Jain, Gaurav Goyal, Malvika Singh, Chittranjan Mishra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-10-01
Series:Delhi Journal of Ophthalmology
Subjects:
Online Access:https://journals.lww.com/10.7869/djo.2012.55
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