单亲二体
印记(心理学)
遗传咨询
基因组印记
遗传学
产前诊断
医学
心理学
生物
怀孕
染色体
胎儿
核型
基因表达
基因
DNA甲基化
作者
Cyto And Genomics Group Of Medical Genetics Branch Of Chinese Medical Association,Ning Liu,Panlai Shi,Li'na Liu,Xiangdong Kong
出处
期刊:PubMed
日期:2024-06-10
卷期号:41 (6): 685-695
标识
DOI:10.3760/cma.j.cn511374-20231113-00244
摘要
Uniparental disomy (UPD)-related imprinting disorders are a group of congenital disorders which can lead to severe birth defects. Their molecular etiology is the occurrence of UPD in the genomic imprinting regions, which may cause disturbed expression of parent-of-origin imprinted genes. With the widespread applications of genetic testing techniques, the prenatal diagnosis of UPD-related imprinted diseases has gradually become clinical routines. However, due to the complicated pathogenesis of such disorders, currently there is still a lack of standards and norms for the understanding, diagnosis, management and genetic counseling. By referring to the relevant guidelines and consensus, the latest progress of research, and opinions from experts in the relevant fields, the writing group has formulated a consensus over the prenatal diagnosis and genetic counseling for UPD-related imprinting disorders, with an aim to provide a more accurate and rational evaluation in prenatal clinics.
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