在LAMB2相关疾病中对临床特征和基因型-表型相关性进行系统审查
Ryota Suzuki1,2, Nana Sakakibara1, Yuta Ichikawa1
1Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Kidney international reports
|September 14, 2023
概括
皮尔森综合征是由LAMB2变体引起的,呈现出不同的表型. 切断LAMB2变体显著加速病的进展,突出显示了这种罕见疾病中的基因型-表型相关性.
科学领域:
- 遗传学 是一个遗传学.
- 腎臟病學 (nephrology) 是一種醫學.
- 分子生物学分子生物学
背景情况:
- 拉米宁子单元β-2 (LAMB2) 相关疾病或皮尔森综合征的特征是先天性脏综合征,眼睛和神经肌肉症状.
- 下一代测序 (NGS) 扩大了对LAMB2相关疾病表型的理解.
研究的目的:
- 进行LAMB2变体和相关表型的系统审查.
- 分析LAMB2变异患者的基因型-表型相关性和生存结果.
主要方法:
- 对110名LAMB2变异患者的系统文献综述,包括12例新病例.
- 分析致病变体类型,病严重程度,外症状和末期病 (ESKD) 发病情况.
- 基于变种类型的ESKD发病的生存分析.
主要成果:
- 78%的患者患有先天性瘤综合征;55%的患者在12个月内患有ESKD (中位发病时间为6.0个月).
- 与其他变体 (中位数为60.0个月) 相比,双切断LAMB2变体患者的ESKD进展显著提前 (中位数为1.2个月).
- 在拉米林N端域和该域以外的变异之间,没有观察到病发作或ESKD进展的显著差异.
结论:
- 本综述强调了LAMB2相关疾病的表型多样性.
- 基因型-表型相关性显示,切断LAMB2变体与更快的病进展有关.
相关概念视频
Incomplete Dominance
22.7K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
22.7K
Pleiotropy
40.6K
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,...
40.6K
Lethal Alleles
15.5K
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
15.5K
Genome-wide Association Studies-GWAS
13.6K
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...
13.6K
Pedigree Analysis
84.4K
Overview
84.4K
Lysosomal Hydrolases
3.8K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.8K


