• Users Online: 984
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 
CASE REPORT
Year : 2018  |  Volume : 30  |  Issue : 1  |  Page : 46-47

An unusual case of Waardenburg syndrome in a female child


1 Department of Ophthalmology, Regional Hospital, Kullu, Himachal Pradesh, India
2 Department of Ophthalmology, Dr. bRajendra Prasad Government Medical College, Kangra, Himachal Pradesh, India

Correspondence Address:
Neha Chauhan
C/o Sh. Shashi Kant Sood, Village Dehan, Post Office Maranda, Tehsil Palampur, Kangra - 176 102, Himachal Pradesh
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/kjo.kjo_15_18

Rights and Permissions

Ocular albinism is characterized by congenital nystagmus, reduced visual acuity, hypopigmentation of the iris pigment epithelium and the ocular fundus and foveal hypoplasia. We report a case with clinical manifestations consistent with the phenotypes of WS1. The differentiating feature from uniocular albinism is the presence of dystopia canthorum.


[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
    Viewed2128    
    Printed94    
    Emailed0    
    PDF Downloaded132    
    Comments [Add]    

Recommend this journal