染色体1p36删除综合征:四名患者呈现变量
Chakshu Chaudhry1, Divya Kumari1, Inusha Panigrahi1
1Department of Pediatrics, Genetic Metabolic Unit, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Journal of pediatric genetics
|January 1, 2024
概括
染色体1p36缺失综合征是智力障碍的原因,呈现出各种临床特征. 通过基因测试进行早期诊断有助于预后和计划生育.
科学领域:
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
- 发展生物学 发展生物学
背景情况:
- 染色体1p36缺失综合征是一种与智力障碍相关的遗传疾病,约影响1%的受影响个体.
- 临床表现不同,包括发育迟缓,低血压,,矮身,智力障碍,感官缺陷以及心脏和脏的先天异常.
研究的目的:
- 报告三年来在一家遗传诊所诊断出4例1p36删除综合征的新病例.
- 突出儿童患者1p36删除综合征的可变临床表现.
- 强调早期诊断对于改善患者管理和生殖咨询的重要性.
主要方法:
- 使用下一代测序 (NGS) 对一个患者.
- 在另一位病人身上使用染色体微阵列分析 (CMA).
- 在剩下的两名患者中应用了多重结合依赖探头放大 (MLPA).
主要成果:
- 通过使用不同的遗传测试方法,成功诊断出4例1p36删除综合征的儿科病例.
- 在被诊断的四个儿童中观察到临床表型的显著变化.
- 证实了不同遗传技术在识别1p36删除中的有用性.
结论:
- 1p36删除综合征表现出广泛的临床特征,需要全面的诊断方法.
- 早期发现1p36删除综合征对于准确的预后和明智的生殖计划至关重要.
- 基因检测,包括NGS,CMA和MLPA,在诊断这种疾病方面发挥着至关重要的作用.
相关概念视频
Karyotyping
60.7K
Overview
60.7K
Genomic Imprinting and Inheritance
34.5K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
34.5K
Polytene Chromosomes
10.0K
Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also...
10.0K
Meiosis I
193.6K
Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by...
193.6K
Abnormal Proliferation
4.5K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.5K
Nondisjunction
75.6K
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
75.6K


