先天性前段眼部疾病:基因型-表型相关性和新出现的新机制
Linda M Reis1, Sarah E Seese1, Deborah Costakos1
1Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI, 53226, USA.
Progress in retinal and eye research
|August 3, 2024
概括
遗传因素会影响眼睛的发育,而眼睛的发育中断会导致前部细分障碍 (ASD). 这篇评论探讨了这些复杂的先天性眼睛疾病的遗传原因,基因型-表型相关性和治疗方法.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 是一个遗传学.
- 发展生物学 发展生物学
背景情况:
- 眼睛前部的先天性异常是由于发育过程的中断而产生的.
- 前段障碍 (ASD) 包括诸如无血病,阿森菲尔德-里格异常,先天性角膜不透明性和初级先天性玻璃眼等疾病.
- 遗传因素至关重要,但只有大约50%的自闭症病例得到了遗传诊断,突出了不完全的理解.
研究的目的:
- 审查当前关于ASD遗传因素的知识.
- 讨论基因型-表型相关性和临床表现.
- 探索新的遗传候选人和ASD的新兴治疗方法.
主要方法:
- 对遗传因素,临床表现和与ASD相关的功能数据的文献综述.
- 对25个与自闭症相关的因素的基因型-表型相关性分析.
- 包括新发现的基因和非编码变异.
主要成果:
- 在FOXC1,CYP1B1和PITX2中的致病变体与ASD的广泛谱系有关.
- 对于一些基因,已经确定了表型扩展和多重遗传模式.
- 影响特定领域的非编码变异和等位基因代表了需要进一步研究的新机制.
结论:
- 了解自闭症的遗传基础对于诊断和治疗至关重要.
- 对包括非编码变异在内的新型遗传因素的持续研究至关重要.
- 基因理解的进步为改善先天性眼睛疾病的治疗策略铺平了道路.
关键词:
安尼里迪亚 (Aniridia) 是一个无线的生物.前段失调是因为前段失调.阿克森菲尔德 - 里格尔是什么意思角膜的不透明性 角膜的不透明性异质性 异质性 异质性这就是彼得的异常.主要的先天性阿法基亚.主要的先天性玻璃眼.更多相关视频
07:38Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
Published on: March 30, 2015
9.2K
08:17Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
19.2K
相关概念视频
Genetic Lingo
102.3K
Overview
102.3K
Glaucoma: Overview
530
Glaucoma is an eye condition characterized by increased intraocular pressure that damages the retina and optic nerve, leading to irreversible blindness if left untreated. The human eye has various components, including the cornea, iris, pupil, lens, and optic nerve. Aqueous humor is secreted by the epithelium of the ciliary body in the posterior chamber and flows through the trabecular meshwork and canal of Schlemm, maintaining normal intraocular pressure. The trabecular meshwork and the canal...
530
Photoreceptors and Visual Pathways
6.0K
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,...
6.0K
Pleiotropy
40.3K
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,...
40.3K
Sex-linked Disorders
101.9K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
101.9K
Human Genetics
551
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...
551
