Two Female Siblings With Bietti Crystalline Retinopathy Without Corneal Dystrophy
Journal of the Korean Ophthalmological Society
;
: 1120-1127, 2009.
Artigo
em Coreano
| WPRIM
| ID: wpr-15445
ABSTRACT
PURPOSE:
To report clinical and functional results in two female siblings with Bietti crystalline retinopathy. CASESUMMARY:
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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Angiofluoresceinografia
/
Acuidade Visual
/
Cegueira Noturna
/
Cristalinas
/
Irmãos
/
Olho
Limite:
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
2009
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS