Waardenburg syndrome, Heterochromia iridis, Deaf mutism.

Santosh Kumar Singh1; Sunil Kumar Gupta2; Anand Agarwal3

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2014 Month : October Volume : 3 Issue : 55 Page : 12687-12689

WAARDENBURG SYNDROME TYPE II: A CASE REPORT

Santosh Kumar Singh1, Sunil Kumar Gupta2, Anand Agarwal3

CORRESPONDING AUTHOR:
Dr. Santosh Kumar Singh,
Assistant Professor,
Department of Dermatology,
BRD Medical College,
Gorakhpur.
Email: drsantoshsingh15@gmail.com

ABSTRACT: Waardenburg syndrome is a rare syndrome, characterized by lateral displacement of the medial canthi combined with dystopia of the lacrimal punctum and blepharophimosis, prominent broad nasal root, hypertrichosis of the medial part of the eyebrows, white forelock, heterochromia iridis, and deaf mutism. A four months old girl with waardenburg syndrome type II, who had the characterstic features of the syndrome, is reported.

KEYWORDS: Waardenburg syndrome, Heterochromia iridis, Deaf mutism.