Paunescu K, Preising M N, Janke B, Wissinger B, Lorenz B
Department of Pediatric Ophthalmology, Strabismology, and Ophthalmogenetics, Klinikum, University of Regensburg, Regensburg, Germany.
Ophthalmology. 2007 Jul;114(7):1348-1357.e1. doi: 10.1016/j.ophtha.2006.10.034. Epub 2007 Feb 22.
To describe the genotype-phenotype correlation in a German family with a novel CRX mutation and to perform a comparative analysis of published cases.
Retrospective observational case series, systematic review, and comparative analysis of the literature.
Four related patients with progressive retinal degeneration.
Mutation screening by single-strand polymorphism analysis and direct sequencing. Clinical examination included kinetic visual fields (VFs), 2-color threshold perimetry (2CTP), full-field electroretinography, fundus photography, optical coherence tomography, and fundus autofluorescence (FA) recording.
Visual fields, subjective and objective cone- and rod-specific function, fundus aspect, retinal stratification, and FA.
A novel heterozygous complex mutation (c.816delCACinsAA) in CRX predicting the substitution of 27 C-terminal amino acids by 44 novel amino acids, thus abolishing the OTX tail, was identified in a 2-generation family finally diagnosed with cone-rod dystrophy (CRD), which was confirmed by 2CTP. Patients presented with variability in progression, nystagmus, and nyctalopia. Most of the patients were hyperopic. Electroretinography recordings showed residual rod and mixed cone-rod responses in 2 of the subjects. Age-dependent VF losses followed funduscopic changes of progressive atrophy of the retinal pigment epithelium and neuroretina in the macula and midperiphery marked by disturbed FA. Optical coherence tomography showed decreased central retinal thickness. Comparative analysis of the 131 published data sets revealed 2 groups: patients with early and late onset.
We described a 2-generation family with a novel mutation in CRX. The resulting phenotype is that of CRD with variable age at onset and progression. The phenotype description of previously published cases is conclusive only for CRD.
描述一个携带新型CRX突变的德国家庭中的基因型-表型相关性,并对已发表病例进行比较分析。
回顾性观察病例系列、系统评价及文献比较分析。
四名患有进行性视网膜变性的相关患者。
通过单链多态性分析和直接测序进行突变筛查。临床检查包括动态视野(VF)、双色阈值视野检查(2CTP)、全视野视网膜电图、眼底照相、光学相干断层扫描和眼底自发荧光(FA)记录。
视野、主观和客观的视锥和视杆特异性功能、眼底外观、视网膜分层和FA。
在一个最终被诊断为锥杆营养不良(CRD)的两代家庭中,发现了CRX基因中的一种新型杂合复合突变(c.816delCACinsAA),该突变预测27个C末端氨基酸被44个新氨基酸取代,从而消除了OTX尾部,这一结果通过2CTP得到证实。患者在病情进展、眼球震颤和夜盲方面存在差异。大多数患者为远视。视网膜电图记录显示其中两名受试者有残余的视杆反应和混合的视锥-视杆反应。年龄依赖性视野缺损伴随眼底改变,表现为视网膜色素上皮和黄斑及中周边神经视网膜的进行性萎缩,FA异常。光学相干断层扫描显示中心视网膜厚度降低。对131个已发表数据集的比较分析揭示了两组:早发和晚发患者。
我们描述了一个携带CRX新型突变的两代家庭。由此产生的表型是发病年龄和进展可变的CRD。先前发表病例的表型描述仅对CRD具有决定性意义。