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KMID : 0360220090500071120
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Journal of the Korean Ophthalmological Society
2009 Volume.50 No. 7 p.1120 ~ p.1127
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Two Female Siblings With Bietti Crystalline Retinopathy Without Corneal Dystrophy
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Ha Seung-Min
Yu Hyeong-Gon
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Abstract
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Purpose: To report clinical and functional results in two female siblings with Bietti crystalline retinopathy.
Case summary: Recently, a 48-year-old female with bilateral intraretinal depositions presented with a complaint of decreased visual acuity and night blindness in both eyes. Several tiny glistening yellow intraretinal crystalline depositions were observed. Fluorescein angiography showed a well-demarcated choriocapillaris filling defect and pigment epithelial window defect. Electrophysiologic tests showed decreased amplitude and OCT scans showed fine intraretinal lesions with increased signal intensity. In addition, a 50-year-old female sibling presented with bilateral yellow, intraretinal crystalline depositions. A choriocapillaris filling defect and pigment epithelial window defect in a fluorescein angiography was observed. Electrophysiologic tests showed severely decreased amplitude.
Conclusions: Two female siblings with Bietti crystalline retinopathy are reported.
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KEYWORD
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Bietti crystalline retinopathy, Siblings
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