贝斯特1变异与非典型的黄斑和外围视网膜表型相关
Srinidhi Singuri1,2, Meghan J DeBenedictis1, Elias I Traboulsi1
1Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
Retinal cases & brief reports
|December 18, 2024
概括
贝斯特罗芬-1 (BEST1) 基因中的一种罕见的遗传变异导致了一种独特形式的Best vitelliform黄斑缩症. 这种状况呈现出不典型的外周病变和泛视网膜功能障碍,扩大了对BEST1相关的黄斑缩症的知识.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 遗传学 是一个
- 视网膜疾病 视网膜疾病
背景情况:
- 贝斯特形斑点缩症 (BVMD) 是一种遗传性疾病.
- 超过250种BESTrophin-1 (BEST1) 基因的致病变体与BVMD有关.
- 与罕见的遗传变异相关的表型变异尚未得到充分记录.
研究的目的:
- 描述与罕见的BEST1基因变异相关的表型.
- 报告一家患有自体主导性黄斑发育不良和非典型发现的家庭.
主要方法:
- 在2021年进行的回顾性案例系列.
- 在第三级眼科中心对三个家庭成员的评估.
- 基因分析以确定致病变体.
主要成果:
- 这三名受试者都携带一种异构的BEST1c.227T>A,p.(Ile76Asn) 致病变体.
- 现型包括典型的斑点病变,外围分裂状病变,缩和异常的电网膜图.
- 研究结果表明,除了典型的黄斑参与之外,还存在泛视网膜功能障碍.
结论:
- 这是第一份描述BEST1c.227T>A,p.(Ile76Asn) 变种表型的报告.
- 鉴定出的表型是独一无二的,它结合了BVMD的特征与外围和电网膜学异常.
- 这种变体可能会导致BVMD的泛视网膜功能障碍.
相关概念视频
Genetic Lingo
100.9K
Overview
100.9K
Anatomy of the Eyeball
5.9K
The eye is a spherical, hollow structure composed of three tissue layers. The outer layer — the fibrous tunic, comprises the sclera — a white structure — and the cornea, which is transparent. The sclera encompasses some of the ocular surface, most of which is not visible. However, the 'white of the eye' is distinctively visible in humans compared to other species. The cornea, a clear covering at the front of the eye, enables light penetration. The eye's middle...
5.9K
Photoreceptors and Visual Pathways
5.6K
At the molecular level, visual signals trigger transformations in photopigment molecules, resulting in changes in the photoreceptor cell's membrane potential. The photon's energy level is denoted by its wavelength, with each specific wavelength of visible light associated with a distinct color. The spectral range of visible light, classified as electromagnetic radiation, spans from 380 to 720 nm. Electromagnetic radiation wavelengths exceeding 720 nm fall under the infrared category,...
5.6K
Pleiotropy
39.7K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
39.7K


