Suppr超能文献

羊膜穿刺术时染色体重排携带者不平衡后代的风险:来自美国和加拿大实验室的数据。

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

作者信息

Daniel A, Hook E B, Wulf G

机构信息

Cytogenetics and Molecular Cell Biology Laboratory, Shodair Children's Hospital, Helena, Montana.

出版信息

Am J Med Genet. 1989 May;33(1):14-53. doi: 10.1002/ajmg.1320330105.

Abstract

Data on 1,237 prenatal (amniocyte) diagnoses in cases of familial chromosome rearrangements were collated from 79 American and Canadian laboratories. These were added to European data (Daniel et al: Prenatal Diagn 6:315-350, 1986) on 596 reciprocal translocations (rcp) from 71 collaborative laboratories. The total data set was examined for relationships between balanced or unbalanced result and mode of ascertainment, sex of carrier parent, chromosomes involved, and (in cases of reciprocal translocations and pericentric inversions) for potential or actual chromosome imbalance size (% haploid autosome length). Risk rates for unbalanced segregants were markedly dissimilar. These ranged from approximately 50% down to essentially a negligible risk. The risk was approximately 50% for carriers of the following: complex chromosome rearrangements (ccr); insertions (ins); and for 2:2 segregating rcp ascertained by mode 1 (term unbalanced proband) with small imbalance segments. Pooled carriers (either sex) of 2:2 segregating rcp of mode 1 had a risk of 20-25% whereas female Robertsonian (rob) translocation (D;21) carriers and pericentric inversion (pii) carriers of pii with small distal segments had a risk of 10-15%. Pooled 2:2 segregating rcp carriers ascertained by mode 2 (a couple with recurrent miscarriages) and male carriers of rob (D;21) had a risk of 1.5-5%. The risk of unbalanced segregants was 1-2% (in this data) for male and female rob (13;14) carriers and for pooled pericentric inversion carriers. However, for carriers of most "type" (recurrent breakpoints) pii, for all paracentric inversions, and (as expected) for rob not involving 13 or 21, there were no term unbalanced progeny. For 2:2 segregating reciprocal translocations plots were prepared that could be used to determine broad risk groups for carriers of such rcp. In 3:1 segregating rcp there were 3.3 times fewer male than female carriers, whereas there were 1.3 times fewer male carriers in 2:2 segregating rcp. In 2:2 segregating rcp there is little effect on the fertility of male carriers and risks of unbalanced progeny were found to be equal to those for female carriers, whereas in the 3:1 segregating rcp, risks were much less for male as compared to female carriers. This indicates that 3:1 segregating rep are more similar to Robertsonian translocations in their greater effect on the fertility of male carriers.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

从79个美国和加拿大实验室收集了1237例家族性染色体重排病例的产前(羊水细胞)诊断数据。这些数据与欧洲71个合作实验室提供的596例相互易位(rcp)数据(Daniel等人:《产前诊断》6:315 - 350,1986年)合并。对整个数据集进行了检查,以确定平衡或不平衡结果与确定方式、携带染色体的亲本性别、涉及的染色体之间的关系,以及(在相互易位和臂间倒位的情况下)潜在或实际染色体不平衡大小(单倍体常染色体长度的百分比)。不平衡分离体的风险率明显不同。范围从大约50%到基本上可以忽略不计的风险。以下情况的携带者风险约为50%:复杂染色体重排(ccr);插入(ins);以及通过模式1(术语:不平衡先证者)确定的2:2分离rcp且不平衡片段较小。模式1的2:2分离rcp的合并携带者(任何性别)风险为20 - 25%,而女性罗伯逊易位(rob)(D;21)携带者和臂间倒位(pii)且远端片段较小的pii携带者风险为10 - 15%。通过模式2(一对反复流产的夫妇)确定的2:2分离rcp合并携带者和rob(D;21)男性携带者风险为1.5 - 5%。在该数据中,男性和女性rob(13;14)携带者以及合并的臂间倒位携带者不平衡分离体的风险为1 - 2%。然而,对于大多数“类型”(反复出现的断点)pii的携带者、所有臂内倒位,以及(如预期的)不涉及13或21的rob,没有足月的不平衡后代。针对2:2分离的相互易位绘制了图表,可用于确定此类rcp携带者的广泛风险组。在3:1分离的rcp中,男性携带者比女性携带者少3.3倍,而在2:2分离的rcp中男性携带者少1.3倍。在2:2分离的rcp中,男性携带者的生育能力影响较小,发现不平衡后代的风险与女性携带者相等,而在3:1分离的rcp中,男性携带者的风险比女性携带者小得多。这表明3:1分离的rep在对男性携带者生育能力的更大影响方面与罗伯逊易位更相似。(摘要截取自400字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验