| CASE REPORT |
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| Year : 2015 | Volume
: 17
| Issue : 1 | Page : 67-69 |
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Mizuo-Nakamura phenomenon (a rare ocular phenomenon)
S Agrawal, Shreyansh Doshi, AS Parihar, Nikita Sonawane, Merlin Saldanha
Dept of Ophthalmology, INHS, Asvini, Colaba- 400005, Mumbai, India
Correspondence Address:
S Agrawal
Dept of Ophthalmology, INHS, Asvini, Colaba- 400005
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0975-3605.203399
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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.
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