Oculogenetic Unit, Jules-Gonin University Eye Hospital, Lausanne, Switzerland.
Institute for Research in Ophthalmology (IRO), Sion, Switzerland.
Ophthalmic Genet. 2021 Dec;42(6):773-779. doi: 10.1080/13816810.2021.1952620. Epub 2021 Jul 26.
Whereas crystals deposit in the retina, the cornea and limbus in Bietty corneo-retinal dystrophy (BCD) is now well established and documented, only two published cases report their findings in the lens and no cases deep in the lens cortex.
Four consecutive adult patients from three different unrelated families presenting lens crystals associated with advanced genetically confirmed BCD were enrolled with advanced disease and long follow up (>12 years). Demographics, visual acuity, slit lamp biomicroscopy, lens and posterior pole photography, optical coherence tomography (OCT), autofluorescence, and screening for CYP4V2 type of mutation were performed. The setting was Jules Gonin Eye Hospital, Switzerland, between 1.1 2013 and 1.11. 2019.
All patients were European women. The ages ranged from 40 to 81 years. Best Snellen visual acuity ranged from light perception to 1.0. All patients presented with limbus and retinal crystals deposit that disappeared over time and the development of severe chorioretinal atrophy. With long-term follow up, multiple crystal-like deposits appeared in the anterior, posterior lens capsule and cortex. All patients, but one, had homozygous or compound heterozygous mutations in CYP4V2 gene.
To the best of our knowledge, there are no published cases of crystal deposits in the cortex of the lens of patients diagnosed with BCD associated with CYP4V2 gene mutation. This could be a feature of advanced BCD, and their presence in the lens cortex questions the hypothesis of floating deposits from posterior pole although their exact etiology remains to be determined.
在 Bietty 角巩膜视网膜营养不良(BCD)中,晶体沉积于视网膜、角膜和缘部已得到证实和记录,仅有两例文献报道晶体位于晶状体,且未见深层晶状体皮质存在晶体的病例。
本研究纳入了 4 例连续的来自 3 个不相关家族的成年患者,他们均存在与基因确诊的晚期 BCD 相关的晶状体晶体,这些患者疾病进展迅速,随访时间长(>12 年)。收集患者的人口统计学资料、视力、裂隙灯生物显微镜、晶状体和后极摄影、光学相干断层扫描(OCT)、自发荧光,并进行 CYP4V2 基因突变筛查。研究地点为瑞士的 Jules Gonin 眼科医院,时间为 2013 年 1 月至 2019 年 11 月。
所有患者均为欧洲女性,年龄 40 至 81 岁。最佳 Snellen 视力从光感至 1.0 不等。所有患者均存在角膜缘和视网膜晶体沉积,随着时间的推移,这些晶体逐渐消失,出现严重的脉络膜视网膜萎缩。长期随访发现,患者的前、后晶状体囊和皮质出现多个类似晶体的沉积物。除 1 例患者外,其余患者均存在 CYP4V2 基因突变的纯合子或复合杂合子。
据我们所知,目前尚无与 CYP4V2 基因突变相关的 BCD 患者晶状体皮质存在晶体沉积的文献报道。这可能是晚期 BCD 的特征,尽管其确切病因仍有待确定,但它们在晶状体皮质中的存在质疑了来自后极的漂浮沉积物的假说。