伪虫弹性 - 遗传学,病理生理学和临床表现
Kristina Pfau1, Imre Lengyel2, Jeannette Ossewaarde-van Norel3
1Department of Ophthalmology, University Hospital Basel, Basel, Switzerland; Department of Ophthalmology, University Hospital Bonn, Bonn, Germany.
Progress in retinal and eye research
|May 30, 2024
概括
伪松弹性 (PXE) 是一种遗传性疾病,导致广泛的化. 目前的研究回顾PXE PXE
科学领域:
- 遗传学和分子生物学
- 眼科医生 眼科 眼科
- 皮肤病学 皮肤病学
- 心血管医学 心血管医学
背景情况:
- 伪神弹性 (PXE) 是一种自体逆性遗传多系统性疾病.
- 由ABCC6基因突变引起,导致血无机酸盐 (PPi) 水平降低.
- 皮肤,心血管系统和眼睛的弹性纤维逐渐化.
研究的目的:
- 提供对目前对PXE的理解的全面审查.
- 详细介绍多系统性表现,重点关注眼部的发现.
- 讨论对致病性PXE治疗的当前和未来临床试验.
主要方法:
- 关于Pseudoxanthoma elasticum现有研究的文献综述.
- 综合基因基础,临床表型和治疗策略的信息.
- 对眼部表现的分析,包括形态和功能上的后果.
主要成果:
- PXE会影响多个器官系统,尤其是眼睛,皮肤和血管系统.
- 眼部表现包括色皮肤,血管状条纹和彗星尾部病变,往往导致二级黄斑新血管化.
- 目前还没有治愈疗法,但有前途的治疗方法正在开发中.
结论:
- PXE是一种复杂的遗传性疾病,具有显著的多系统影响,特别是在视力上.
- 开发有效的结果措施对于推进PXE临床试验至关重要.
- 目前正在进行的研究和临床试验为未来PXE的致病疗法提供了希望.
关键词:
ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC6ABCC布鲁克的膜是布鲁克的膜在PXE中,PXE是PXE.伪索索马弹性 (Pseudoxanthoma elasticum) 是一种类型的虫.相关概念视频
Pleiotropy
40.4K
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,...
40.4K
Changes in Skin Color: Clinical Perspectives
1.9K
The first thing a clinician sees is the skin, so the examination of the skin should be part of any thorough physical examination. Most skin disorders are relatively benign, but a few, including melanomas, can be fatal if untreated. A couple of the more noticeable disorders, albinism and vitiligo, affect the appearance of the skin and its accessory organs.
Albinism
Albinism is a genetic disorder that affects (completely or partially) the coloring of skin, hair, and eyes. The defect is primarily...
Albinism
Albinism is a genetic disorder that affects (completely or partially) the coloring of skin, hair, and eyes. The defect is primarily...
1.9K
Nucleotide Excision Repair
3.5K
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.5K
Epistasis
46.7K
In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
46.7K
Skin Cancer
4.1K
Skin cancer is a type of cancer that occurs when there is an abnormal growth of skin cells, usually triggered by damage to the DNA within the skin cells. It is primarily caused by exposure to ultraviolet (UV) radiation from the sun or artificial sources like tanning beds. Skin cancer is the most common type of cancer worldwide, and its incidence continues to rise.
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
4.1K
X-linked Traits
54.9K
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
54.9K


