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مقاله
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Abstract
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Title:
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Oculocutaneous Albinism associated with Fuchs' heterochromic uveitis: a case report
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Author(s):
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Farzan Kianersi,Heshmatollah Ghanbari,Azadeh Mohammadi,Zahra Naderi Beni,Afsaneh Naderi Beni
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Presentation Type:
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Poster
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Subject:
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Posterior Segment and Uveitis
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Others:
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Presenting Author:
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Name:
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Afsaneh Naderi Beni
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Affiliation :(optional)
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Isfahan University of Medical Sciences
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E mail:
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a_naderibeni@yahoo.com
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Phone:
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2264021
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Mobile:
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09133813009
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Purpose:
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: To report the first case of oculocoutaneous albinism associated with Fuchs' heterochromic iridocyclitis .
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Methods:
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A 60-year-old man who was a known case of oculocutaneous albinism was referred to our department with progressive bilateral reduction of vision .
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Results:
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: Visual acuity was 20/400 OD and 50 cm OS.Biomicroscopic examination OD demonstrated Iris transillumination and moderate nuclear sclerosis cataract and OS demonstrated small translucent keratic precipitates scattered over the entire endothelium and minimal aqueous flare and cells, Diffuse iris atrophy and hyperchromia , aphakia with no capsular remnant, Mild vitreous condensation. Fundus examination demonstrated an albino fundus with foveal hypoplasia
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Conclusion:
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We describe the first reported case of oculocoutaneous albinism associated with Fuchs' heterochromic iridocyclitis . This may be a co-incidence or might have occurred due to a defect in embryonic ocular development
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Attachment:
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