Volume 20, Number 2 (July 2013)                   J Birjand Univ Med Sci. 2013, 20(2): 206-210 | Back to browse issues page


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Yaghoobi G, Hosseini Rad S A. Fuchs uveitis,heterochromia,and uveitis as a coincidental finding in a case . J Birjand Univ Med Sci.. 2013; 20 (2) :206-210
URL: http://journal.bums.ac.ir/article-1-1297-en.html

1- Associate professor, ophthalmology department school of medicine, Birjand University of Medical Sciences, Birjand, Iran
2- Assistant Professor, school of medicine, Birjand University of Medical Sciences, Birjand, Iran
Abstract:   (6442 Views)

   The classical clinical triad of retinitis pigmentosa is arteriolar attenuation , retinal bone-spicule pigmentation and waxy disc pallor.

  A 33 year old female patient is introduced here. She had unilateral posterior subcapsular cataract, heterochromic iris, and uveitis.The patient also suffered night blindness , had a family history of low vision ,and reduced visual acuity in her right eye. After the best correction, visual acuity was: OD=20.200 and OS=20.20 (with-1.5 spher-0.50cyl x 170). Anterior segment examination revealed trace cell with diffused moderate keratic precipitate and heterochoromia with posterior subcapsular cataract .But the examination revealed a normal condition in the left eye. Both eyes had characteristic retinal changes of retinitis pigmentosa. Retinitis pigmentosa can be associated with Fuch’s- like uveitis sporadicallybut Fuch’s heterochromic uveitis of affected pedigree was not found.

  

 

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Type of Study: Case Report | Subject: General
Received: 2012/11/23 | Accepted: 2013/09/3 | Published: 2014/09/22

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