基底细胞瘤综合征患者视通路的电生理研究。

IF 3.1 Q1 OPHTHALMOLOGY Eye and Brain Pub Date : 2021-03-29 eCollection Date: 2021-01-01 DOI:10.2147/EB.S281135
Antonietta Moramarco, Ludovico Alisi, Alessandro Lambiase, Sandra Giustini, Luca Lucchino, Emanuele Miraglia, Vincenzo Roberti, Marcella Nebbioso
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引用次数: 0

摘要

简介:Gorlin-Goltz综合征(GGS)也被称为瘤状基底细胞癌综合征(NBCCS),是一种复杂的罕见遗传疾病,具有广泛的临床和放射学表现。眼科的改变一直有报道,但尚未有关于最终模式视觉诱发电位(pVEPs)异常的研究发表。目的:本研究的目的是通过模式逆转VEPs评估一组NBCCS患者视神经通路的功能,在彻底排除了先前存在的眼部和视神经通路病变的受试者后。方法:本研究招募19例NBCCS患者(31眼)和20例健康对照(40眼)。所有受试者通过小(120')、中(60')和大(15')检查尺寸刺激的pvep对视神经通路的功能进行了评估。结果:与对照组相比,NBCCS患者黄斑通路功能的传递有统计学意义的改变。PVEPs分析证实P100成分的振幅降低和潜伏期增加,表明即使在没有眼部临床表现的情况下也可能涉及视觉通路。结论:视觉通路可能受到亚临床髓鞘形成缺陷的影响,直接由遗传改变决定,以及该综合征典型的神经异常。进一步的研究是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Electrophysiological Study of Visual Pathways in Nevoid Basal Cell Carcinoma Syndrome Patients.

Introduction: Gorlin-Goltz syndrome (GGS) also known as nevoid basal cell carcinoma syndrome (NBCCS) is a complex rare genetic disorder characterized by a wide range of clinical and radiological manifestations. Ophthalmological alterations have always been reported, but no study on the eventual pattern visual evoked potentials (pVEPs) abnormalities has yet been published.

Purpose: The purpose of the study was to evaluate the functionality of the optic pathways in a group of NBCCS patients through pattern reversal VEPs, after a thorough exclusion of subjects with preexisting ocular and optic pathways pathologies.

Methods: Nineteen NBCCS patients (31 eyes) and 20 healthy controls (40 eyes) have been recruited for this study. All subjects underwent an evaluation of the functionality of the optic pathways through pVEPs with small (120'), medium (60'), and large (15') check size stimulation.

Results: NBCCS patients showed a statistically significant alteration in the transmission of the macular pathway function when compared to controls. PVEPs analysis confirmed a reduced amplitude and an increased latency of the P100 component, suggesting an involvement of the visual pathway even in the absence of ocular clinical manifestations.

Conclusion: Visual pathways may have been affected both by a subclinical myelination deficit, determined directly by the genetic alteration, as well as by neurological abnormalities typical of this syndrome. Further studies are warranted.

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来源期刊
Eye and Brain
Eye and Brain OPHTHALMOLOGY-
CiteScore
7.90
自引率
2.30%
发文量
12
审稿时长
16 weeks
期刊介绍: Eye and Brain is an international, peer-reviewed, open access journal focusing on basic research, clinical findings, and expert reviews in the field of visual science and neuro-ophthalmology. The journal’s unique focus is the link between two well-known visual centres, the eye and the brain, with an emphasis on the importance of such connections. All aspects of clinical and especially basic research on the visual system are addressed within the journal as well as significant future directions in vision research and therapeutic measures. This unique journal focuses on neurological aspects of vision – both physiological and pathological. The scope of the journal spans from the cornea to the associational visual cortex and all the visual centers in between. Topics range from basic biological mechanisms to therapeutic treatment, from simple organisms to humans, and utilizing techniques from molecular biology to behavior. The journal especially welcomes primary research articles or review papers that make the connection between the eye and the brain. Specific areas covered in the journal include: Physiology and pathophysiology of visual centers, Eye movement disorders and strabismus, Cellular, biochemical, and molecular features of the visual system, Structural and functional organization of the eye and of the visual cortex, Metabolic demands of the visual system, Diseases and disorders with neuro-ophthalmic manifestations, Clinical and experimental neuro-ophthalmology and visual system pathologies, Epidemiological studies.
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