[艾勒斯-丹洛斯综合征的眼部表现和遗传方面]
L V Reznikova1, T Yu Degtyarevskaya1, M B Kuchminskaya1
1I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.
Vestnik oftalmologii
|July 1, 2025
概括
埃勒斯-丹洛斯综合征 (EDS) 是一组影响眼睛的遗传性结缔组织疾病. 本综述详细介绍了EDS类型与眼部症状,诊断标准,以及预防严重视力丧失的管理.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 是一个遗传学.
- 类风湿病学 类风湿病学
背景情况:
- 埃勒斯-丹洛斯综合征 (EDS) 包括影响原蛋白合成的遗传性结合组织疾病.
- 在几种EDS类型中,眼部表现显著,影响患者的预后.
- 了解这些联系对于早期诊断和管理至关重要.
研究的目的:
- 审查有关埃勒斯-丹洛斯综合征与眼科症状的当前数据.
- 概述各种EDS类型的诊断标准和眼部症状.
- 强调基因检测和及时治疗,以预防严重的眼部并发症.
主要方法:
- 对埃勒斯-丹洛斯综合征和眼科现有数据的文献综述.
- 对EDS亚型的眼科诊断标准的分析.
- 识别眼部症状和管理策略.
主要成果:
- 专注于眼部参与的EDS类型:脆性角膜综合征,囊性,肌肉收缩性,脊髓质疏松性,皮肤性,血管性和古典性.
- 详细介绍了眼科诊断标准和相关的眼部症状.
- 该审查强调了对致病基因的遗传鉴定所面临的挑战.
结论:
- 精确诊断EDS与眼部发现需要分子遗传测试.
- 及时治疗对于纠正视觉障碍和预防严重并发症,如球裂和视网膜脱落至关重要.
- 对于患有EDS相关眼睛疾病的患者来说,全面的治疗策略至关重要.
相关概念视频
Genetic Lingo
105.0K
Overview
105.0K
Cardiomyopathy III: Hypertrophic Cardiomyopathy
64
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
64
Human Genetics
738
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
The complex relationship between genetics and psychology is observable through common biological components such...
738
Genome-wide Association Studies-GWAS
14.4K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
14.4K
Pleiotropy
41.2K
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,...
41.2K
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies
70
The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
70


