CLINICAL-FEATURES OF AFFECTED MALES WITH X-LINKED OCULAR ALBINISM

被引:64
作者
CHARLES, SJ
GREEN, JS
GRANT, JW
YATES, JRW
MOORE, AT
机构
[1] ADDENBROOKES HOSP,DEPT OPHTHALMOL,CAMBRIDGE CB2 2QQ,ENGLAND
[2] ADDENBROOKES HOSP,DEPT HISTOPATHOL,CAMBRIDGE CB2 2QQ,ENGLAND
[3] ADDENBROOKES HOSP,DEPT CLIN GENET,CAMBRIDGE CB2 2QQ,ENGLAND
[4] UNIV CAMBRIDGE,DEPT PATHOL,CAMBRIDGE,ENGLAND
[5] MEM UNIV NEWFOUNDLAND,ST JOHNS A1C 5S7,NEWFOUNDLAND,CANADA
基金
英国惠康基金;
关键词
D O I
10.1136/bjo.77.4.222
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Seventy four males affected by X linked ocular albinism (XLOA) from 19 pedigrees were examined to assess phenotypic variation and visual prognosis. Nystagmus was present in all cases except one. Best visual acuity ranged from 6/9 to 6/60; 79.7% could see 6/36 or better; most could read N5. Marked iris translucency and foveal hypoplasia were present in all cases. Posterior embryotoxon was present in 30% and dysplastic optic discs were often seen. Pigmentation of the posterior pole was associated with better visual acuity. XLOA is under-diagnosed: almost 20% of cases had been previously diagnosed as having congenital nystagmus until reviewed in this study.
引用
收藏
页码:222 / 227
页数:6
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