一个严重的脊髓甲基细胞失生症病例,阿尔及利亚类型,在COL2A1中有两个突变
Francisco Cammarata-Scalisi1, Uta Matysiak2, Colin E Willoughby3
1Departamento of Pediatrics, Regional Hospital of Antofagasta, Antofagasta, Chile.
Journal of pediatric genetics
|January 1, 2024
概括
阿尔及利亚类型的脊柱形状细胞质变异,一种罕见的骨疾病,与COL2A1基因突变有关. 这个案例突出了一个具有特征特征和新奇突变的患者.
科学领域:
- 遗传学 遗传学 是一个
- 骨发育不良症 骨发育不良症
- 分子生物学分子生物学
背景情况:
- 阿尔及利亚类型的脊柱形状细胞缺血症是一种不常见的自体主导骨缺血症.
- 它是由COL2A1基因中的异构基因突变引起的.
研究的目的:
- 报告一名5岁男孩患有阿尔及利亚类型的脊柱形状细胞失质症病例.
- 为了分析与这个患者的病情相关的遗传突变.
主要方法:
- 对患者进行临床检查和放射学评估.
- 对 COL2A1 基因进行基因分析,以确定突变.
主要成果:
- 这位患者身高矮,严重的脊椎病,腰部超 lordosis,短干,和真体 valgum.
- 放射学发现包括平底,不规则的甲基细胞辐射和角骨折.
- 鉴定出一种病原性突变 (c.3275G>A;p.Gly1092Asp) 在前列子47中,以及一种未知意义的变异 (c.1366-13C>A) 在 COL2A1 基因的内突21中.
结论:
- 鉴定到的 COL2A1 基因突变与阿尔及利亚类型表型的 Spondylometaphyseal 发育不良有关.
- 内部21的变异可能会通过潜在地破坏拼接来影响表型严重性.
相关概念视频
Lethal Alleles
15.4K
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...
15.4K
Alternative RNA Splicing
21.2K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
21.2K
Multiple Allele Traits
34.2K
The Concept of Multiple Allelism
34.2K
Translation
14.9K
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
Translation Produces the Building Blocks of Life
Proteins are...
14.9K
Inborn Errors of Metabolism
161
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
161
Incomplete Dominance
22.6K
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.
22.6K


