一种新型的EDA变体,在一个中国家庭中引起X结合的低性外皮形
Limin Yao1, Lilan Wan1, Yunhong Lin2
1Department of Medical Genetics, NHC Key Laboratory of Healthy Birth and Birth Defect Prevention in Western China, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.
BMC pregnancy and childbirth
|August 8, 2025
概括
产前超声波可以有效地选外皮发育不良. 发现了一种新的EDA基因变异,有助于X链HED的诊断和生殖选择.
科学领域:
- 遗传学 是一个遗传学.
- 医学诊断 医学诊断 医学诊断
- 产前医学产前医学
背景情况:
- 缺水性外皮形症 (HED) 是一种罕见的遗传疾病,影响外皮发育.
- 产前诊断HED是具有挑战性的,因为稀有性和有限的特定超声波特征.
- 许多导致HED的基因变异仍然未被确定.
研究的目的:
- 评估产前超声波作为HED的查工具.
- 为了识别与X链接HED (XLHED) 相关的新型遗传变异.
- 在HED案件中,为生殖决策提供诊断支持.
主要方法:
- 妊娠23周的胎儿超声波显示了薄膜骨和缺少牙生殖组织.
- 基于trio的全外体序列测定在试验体和胎儿中发现了一种新的EDA基因变异 (c.806G>T,p.Gly269Val).
- 桑格测序证实了胎儿皮肤组织在终止后的EDA突变.
主要成果:
- 产前超声检查发现了暗示HED的特征,包括未发达的膜骨和牙细菌.
- 发现了一种新的可能致病性EDA基因变异,扩大了已知的XLHED突变谱.
- 在胎儿中由于已识别的EDA变异而导致的HED的遗传确认.
结论:
- 产前超声波是一种有效的查方法,可以在怀孕期间检测HED.
- 鉴定一种新的EDA变种有助于准确诊断XLHED.
- 这项研究支持受HED影响的家庭做出明智的生殖决策.
更多相关视频
相关概念视频
Exon Recombination
3.7K
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...
3.7K
X-linked Traits
55.3K
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”.
55.3K
Sex-linked Disorders
103.0K
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.
103.0K
Genetic Lingo
104.7K
Overview
104.7K
Incomplete Dominance
25.4K
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.
25.4K
Pleiotropy
41.1K
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,...
41.1K


