mizuo-nakamura phenomenon (a rare ocular phenomenon)

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ID: 247662
2015
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Abstract
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.
Reference Key
agrawal2015journalmizuo-nakamura Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;S Agrawal;Shreyansh Doshi;A S Parihar;Nikita Sonawane;Merlin Saldanha
Journal studia quranika: jurnal studi quran
Year 2015
DOI
10.4103/0975-3605.203399
URL
http://www.marinemedicalsociety.in/article.asp?issn=0975-3605;year=2015;volume=17;issue=1;spage=67;epage=69;aulast=Agrawal;type=0
Keywords
night blindnessnaval sciencemedicine

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