听力损失和外皮异常的新综合症病例与GJB6基因的反复错误变异有关
Badreddine Elmakhzen1,2, Paul Rollier1,3, Clémence Saillard4
1Service de Génétique Clinique, Centre de Référence CLAD-Ouest, ERN ITHACA, CHU, Rennes, France.
Molecular genetics & genomic medicine
|May 15, 2025
概括
编码为Cx30的GJB6的遗传变异与遗传性听力损失和皮肤问题有关. 一种特定的GJB6变体 (p.Gly59Arg) 与先天性听力损失和超质症有关.
科学领域:
- 遗传学 是一个遗传学.
- 皮肤病学 皮肤病学
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
背景情况:
- 间隙结β6 (GJB6) 基因变异,编码连xin30 (Cx30),是遗传性听力损失的重要贡献者,经常呈现皮肤异常.
- GJB6的变异通常与非综合征性听力损失或水性外皮发育不良 (克劳斯顿型) 相关,后者通常没有聋.
研究的目的:
- 研究儿科患者先天性听力损失和外皮异常的遗传基础.
- 描述与特定的GJB6误解变异相关的表型谱.
主要方法:
- 全基因组测序 (WGS) 用于识别遗传变异.
- 一个13岁的女性患者的临床特征被系统地记录下来.
主要成果:
- 在先天性听力损失,外皮异常 (手掌皮质皮质,手指节,指甲缩) 和GJB6变体 ENST00000647029.1 (GJB6) 之间发现了一种新的关联:c.175G>A (p.
- 这是第三个报告的综合征性听力损失病例,与这种特定的误解变体有关.
结论:
- 在GJB6基因中的p.Gly59Arg变体表现出重叠的表型,突出显示了一系列的临床表现.
- 遗传性听力损失与皮质炎相结合,是与这种GJB6变种相关的关键特征.
更多相关视频
相关概念视频
Pleiotropy
38.3K
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,...
38.3K
Hearing
51.4K
When we hear a sound, our nervous system is detecting sound waves—pressure waves of mechanical energy traveling through a medium. The frequency of the wave is perceived as pitch, while the amplitude is perceived as loudness.
51.4K
Alternative RNA Splicing
20.8K
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...
20.8K
Exon Recombination
3.5K
The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes.
Exon shuffling follows “splice frame rules.” Each exon...
Exon shuffling follows “splice frame rules.” Each exon...
3.5K
Hair Cells
39.5K
Hair cells are the sensory receptors of the auditory system—they transduce mechanical sound waves into electrical energy that the nervous system can understand. Hair cells are located in the organ of Corti within the cochlea of the inner ear, between the basilar and tectorial membranes. The actual sensory receptors are called inner hair cells. The outer hair cells serve other functions, such as sound amplification in the cochlea, and are not discussed in detail here.
39.5K
Sex-linked Disorders
98.6K
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.
98.6K


