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CASE REPORT
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
India
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Source of Support: None, Conflict of Interest: None


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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