异卵性FGFR3 c.138G>一种突变,呈现出无形质和半面微观质的突变
Hyok Jun Kwon1, Lachlan D M Farmer, Mark H Moore
1Cleft and Craniofacial South Australia, Women's and Children's Hospital, Adelaide, South Australia, Australia.
The Journal of craniofacial surgery
|February 16, 2024
概括
本案例研究突出了一个患有无粒细胞增生症和面部微小症的患者,由纤维细胞生长因子受体3突变联系在一起. 这表明这些以前没有联系的疾病可能具有共同的遗传起源.
科学领域:
- 医学遗传学 医学遗传学
- 发展生物学 发展生物学
- 临床病例报告 临床病例报告
背景情况:
- 无粒细胞增生是一种常见的矮体形式,由纤维细胞生长因子受体3 (FGFR3) 基因突变引起.
- 半面微观症是一种影响面部发育的先天性疾病,其病因在很大程度上不明.
- 特定的FGFR3 c.138G>A突变与无质形成有关.
研究的目的:
- 报告一个独特的病例,该病例在一个病人身上结合了阿德罗普拉西亚和半面显微体.
- 基于遗传发现,探索这两种疾病之间的潜在生物联系.
主要方法:
- 对一个被诊断为患有阿德罗普拉西亚和半面显微症的患者的临床表现审查.
- 基因分析以确定纤维细胞生长因子受体3 (FGFR3) 基因的突变.
主要成果:
- 这位患者呈现出阿德罗普拉西亚和半面显微症的临床特征.
- 基因检测显示了一种特定的纤维细胞生长因子受体3 (FGFR3) c.138G>A突变.
结论:
- 这一案例表明了阿孔多普拉西亚和半面显微症之间潜在的,以前未被描述的关联.
- 鉴定到的FGFR3突变提供了一个可信的生物学机制,将这两种疾病的病因联系起来.
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
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
Sex-linked Disorders
102.1K
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.
102.1K
Multiple Allele Traits
34.2K
The Concept of Multiple Allelism
34.2K
Genetic Lingo
102.8K
Overview
102.8K
The Retinoblastoma Gene
4.1K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.1K


