• Users Online: 376
  • 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 
Year : 2015  |  Volume : 17  |  Issue : 1  |  Page : 67-69

Mizuo-Nakamura phenomenon (a rare ocular phenomenon)

Dept of Ophthalmology, INHS, Asvini, Colaba- 400005, Mumbai, India

Correspondence Address:
S Agrawal
Dept of Ophthalmology, INHS, Asvini, Colaba- 400005
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0975-3605.203399

Rights and Permissions

Oguchi disease, first described in 1907, is a rare autosomal recessive disorder characterized by congenital stationary night blindness with a unique morphological and functional abnormality of the retina. The cause, though largely unknown, is associated with ARRESTIN and RHODOPSIN KINASE gene defects. This is a case report of a 20 yr old male patient of Oguchi disease who presented with classical symptoms and morphological features in the form of Mizuo phenomenon.

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
    PDF Downloaded110    
    Comments [Add]    

Recommend this journal