Waardenburg syndrome: A rare case

Waardenburg syndrome: A rare case

Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherited. Varying in prevalence from 1:42000 to 1:50,000, it compromises approximately 2-5% of congenital deaf children. The syndrome is not expressed in its complete form, in about 20% cases, which adds for...

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Bibliographic Details
Main Authors: Shivlal M Rawlani, Roshani Ramtake, Ajab Dhabarde, Sudhir S Rawlani
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Oman Journal of Ophthalmology
Subjects:
Hearing loss
heterochromia
hypopigmentation
Waardenburg syndrome
white forelock
Online Access:http://www.ojoonline.org/article.asp?issn=0974-620X;year=2018;volume=11;issue=2;spage=158;epage=160;aulast=Rawlani

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http://www.ojoonline.org/article.asp?issn=0974-620X;year=2018;volume=11;issue=2;spage=158;epage=160;aulast=Rawlani

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