与DYNC2H1相关的短肋胸部形症的表型异质性:产前指标和产后结果
Nikhil Pattani1, Nour Elkhateeb2, Aakash Joshi1
1Department of Clinical Genetics, South West Thames Regional Genetic Services, London, UK.
Journal of medical genetics
|April 18, 2025
概括
与DYNC2H1相关的短肋胸部发育不良 (SRTD) 呈现出各种症状和严重程度. 早期的产前呈现和股骨缩短可以预测较差的结果,但基因型不能可靠地预测表型.
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
- 医学遗传学 医学遗传学
背景情况:
- 与DYNC2H1相关的短肋胸部形 (SRTD) 是一种罕见的遗传骨疾病.
- 它的特点是胸部狭窄,肋骨短,长骨缩短,以及多爪症.
- 临床表现的显著变化和对基因型-表型相关性的有限理解.
研究的目的:
- 调查DYNC2H1相关的SRTD中的基因型-表型相关性.
- 分析产前超声波发现和临床表型.
- 为了确定疾病严重程度和预后的预测因素.
主要方法:
- 对已确认的DYNC2H1相关SRTD病例的回顾性研究.
- 数据收集包括人口统计,临床表现,产前超声波,骨调查和遗传变异分析.
- 分析了来自八个家庭的九个人.
主要成果:
- 现型严重程度从轻度到致命的范围.
- 较早的产前表现和股骨缩短/鞠躬预测预后较差.
- 没有明确的基因型-表型相关性;报告了七种新的DYNC2H1变体.
结论:
- 与DYNC2H1相关的SRTD表现出显著的表型变异性.
- 基因型不能可靠地预测表型.
- 妊娠呈现时间与严重程度相关,提供了一些预测价值.
更多相关视频
09:34A Combinatorial Single-cell Approach to Characterize the Molecular and Immunophenotypic Heterogeneity of Human Stem and Progenitor Populations
Published on: October 25, 2018
6.6K
09:21Author Spotlight: Generating Neuronal Phenotypic Profiles - A Protocol to Culture and Image Human Midbrain Dopaminergic Neurons
Published on: July 7, 2023
1.4K
相关概念视频
Genetic Variation
236
Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles,...
Genes exist in different versions called alleles,...
236
Multiple Allele Traits
33.8K
The Concept of Multiple Allelism
33.8K
Background and Environment Affect Phenotype
6.4K
Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as temperature, oxygen availability, presence of mutagens, that can alter an organism’s phenotype.
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
6.4K
Genetic Lingo
98.4K
Overview
98.4K
Epistasis
43.5K
In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
43.5K
Epistasis Analysis
4.8K
Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
4.8K
