Ophthalmic Laboratories & Department of Ophthalmology, Translational Neuroscience Center, West China Hospital, Sichuan University, Chengdu, Sichuan Province, People's Republic of China.
PLoS One. 2012;7(5):e33673. doi: 10.1371/journal.pone.0033673. Epub 2012 May 31.
Retinitis pigmentosa (RP) is a heterogeneous group of progressive retinal degenerations characterized by pigmentation and atrophy in the mid-periphery of the retina. Twenty two subjects from a four-generation Chinese family with RP and thin cornea, congenital cataract and high myopia is reported in this study. All family members underwent complete ophthalmologic examinations. Patients of the family presented with bone spicule-shaped pigment deposits in retina, retinal vascular attenuation, retinal and choroidal dystrophy, as well as punctate opacity of the lens, reduced cornea thickness and high myopia. Peripheral venous blood was obtained from all patients and their family members for genetic analysis. After mutation analysis in a few known RP candidate genes, exome sequencing was used to analyze the exomes of 3 patients III2, III4, III6 and the unaffected mother II2. A total of 34,693 variations shared by 3 patients were subjected to several filtering steps against existing variation databases. Identified variations were verified in the rest family members by PCR and Sanger sequencing. Compound heterozygous c.802-8_810del17insGC and c.1091-2A>G mutations of the CYP4V2 gene, known as genetic defects for Bietti crystalline corneoretinal dystrophy, were identified as causative mutations for RP of this family.
色素性视网膜炎(RP)是一组异质性的进行性视网膜变性,其特征为视网膜中、周边部色素沉着和萎缩。本研究报道了一个四代中国家族的 22 名 RP 患者,他们还伴有薄角膜、先天性白内障和高度近视。所有家族成员均接受了全面的眼科检查。该家族的患者表现为视网膜上呈骨刺状的色素沉着、视网膜血管衰减、视网膜和脉络膜营养不良以及晶状体点状混浊、角膜变薄和高度近视。从所有患者及其家庭成员中采集外周静脉血进行基因分析。在对少数已知的 RP 候选基因进行突变分析后,对 3 名患者 III2、III4、III6 和未受影响的母亲 II2 的外显子组进行了外显子组测序分析。将 3 名患者共有的 34693 个变异体经过现有变异数据库的多步过滤,确定候选变异体。通过 PCR 和 Sanger 测序在其余家族成员中验证了这些变异体。CYP4V2 基因的 c.802-8_810del17insGC 和 c.1091-2A>G 复合杂合突变被确定为该家族 RP 的致病突变,这两种突变已知是 Bietti 结晶状角膜视网膜营养不良的遗传缺陷。