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患有X连锁眼白化病的男性患者的临床特征。

Clinical features of affected males with X linked ocular albinism.

作者信息

Charles S J, Green J S, Grant J W, Yates J R, Moore A T

机构信息

Addenbrooke's Hospital, Cambridge Department of Ophthalmology.

出版信息

Br J Ophthalmol. 1993 Apr;77(4):222-7. doi: 10.1136/bjo.77.4.222.

Abstract

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.

摘要

对来自19个家系的74名患有X连锁眼部白化病(XLOA)的男性进行了检查,以评估表型变异和视觉预后。除1例病例外,所有病例均存在眼球震颤。最佳视力范围为6/9至6/60;79.7%的患者视力可达6/36或更好;大多数患者能读出N5。所有病例均存在明显的虹膜半透明和黄斑发育不全。30%的患者存在后胚胎环,且常可见发育异常的视盘。后极部色素沉着与较好的视力相关。XLOA的诊断不足:在本研究重新评估之前,近20%的病例曾被诊断为先天性眼球震颤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8589/504486/9dc467eb9a65/brjopthal00040-0028-a.jpg

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