Giant retinal tear and retinal detachment with underlying retinitis pigmentosa and hearing loss

被引:13
作者
Kim, RY
Schwartz, SD
Heckenlively, JR
Gregor, ZJ
Cooling, RJ
机构
[1] MOORFIELDS EYE HOSP, VITREORETINAL UNIT, LONDON, ENGLAND
[2] JULES STEIN EYE INST, LOS ANGELES, CA 90024 USA
关键词
giant retinal tear; hearing loss; retinal detachment; retinitis pigmentosa; Usher syndrome;
D O I
10.1038/eye.1996.163
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Few retinal detachments have been described in patients,vith retinitis pigmentosa and allied retinal disorders, with only two cases (both with hearing loss) reported in association with giant retinal tears, To further characterise clinical characteristics of giant retinal tear associated with retinitis pigmentosa, we reviewed the course of four eyes of three patients, Unexpectedly, all three individuals also suffered from congenital sensorineural hearing loss, One suffered from associated myopathy. Despite aggressive surgical management, three of the four eyes became blind, The diagnosis of retinal detachment preceded the diagnosis of photoreceptor dystrophy in two of the three patients, To date, giant retinal tears occurring with underlying retinitis pigmentosa have been described in five young individuals, all of whom had associated congenital sensorineural hearing loss.
引用
收藏
页码:697 / 700
页数:4
相关论文
共 19 条
[1]  
Arakawa T, 1975, FOLIA OPHTHALMOL JPN, V26, P1036
[2]  
Auvert B, 1973, Bull Soc Ophtalmol Fr, V73, P1159
[3]  
Bartkowska-Orlowska M, 1982, Klin Oczna, V84, P251
[4]  
EDWARDS RS, 1985, T OPHTHAL SOC UK, V104, P315
[5]  
Freeman H M, 1978, Trans Am Ophthalmol Soc, V76, P343
[6]   EXPRESSION IN COCHLEA AND RETINA OF MYOSIN VIIA, THE GENE-PRODUCT DEFECTIVE IN USHER SYNDROME TYPE 1B [J].
HASSON, T ;
HEINTZELMAN, MB ;
SANTOS-SACCHI, J ;
COREY, DP ;
MOOSEKER, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (21) :9815-9819
[7]  
Johnston G P, 1981, Retina, V1, P223
[8]  
JOHNSTON ME, 1985, CAN J OPHTHALMOL, V20, P16
[9]   A GENE FOR USHER SYNDROME TYPE-I (USH1A) MAPS TO CHROMOSOME-14Q [J].
KAPLAN, J ;
GERBER, S ;
BONNEAU, D ;
ROZET, JM ;
DELRIEU, O ;
BRIARD, ML ;
DOLLFUS, H ;
GHAZI, I ;
DUFIER, JL ;
FREZAL, J ;
MUNNICH, A .
GENOMICS, 1992, 14 (04) :979-987
[10]  
KIMBERLING WJ, 1995, AM J HUM GENET, V56, P216