Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts 962
CASE REPORT
Year : 2015  |  Volume : 6  |  Issue : 1  |  Page : 89-91

Ocular manifestation of the Alport syndrome: A case report


Department of Ophthalmology, Chettinad Hospital and Research Institute, Tamil Nadu, India

Correspondence Address:
Charanya Chendilnathan
A 401 Urbanville, Velachery Main Road, Velachery, Chennai - 600 042
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0975-9727.146476

Rights and Permissions

The Alport syndrome is a rare genetic disorder characterized by hematuria, sensorineural deafness, and ocular manifestations. The Alport syndrome accounts for 0.3 to 2.3% of end-stage kidney disease in young males and children. Here we report a case of the Alport syndrome, with all the characteristic features.


[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
    Viewed2157    
    Printed55    
    Emailed0    
    PDF Downloaded153    
    Comments [Add]    

Recommend this journal