垂体腺瘤Prader-Willi患者母体来源的同染色体15q。

D Bettio, D Giardino, N Rizzi, P Riva, L Volpi, E Barantani, A Tagliaferri, L Larizza
{"title":"垂体腺瘤Prader-Willi患者母体来源的同染色体15q。","authors":"D Bettio,&nbsp;D Giardino,&nbsp;N Rizzi,&nbsp;P Riva,&nbsp;L Volpi,&nbsp;E Barantani,&nbsp;A Tagliaferri,&nbsp;L Larizza","doi":"10.1017/s000156600000132x","DOIUrl":null,"url":null,"abstract":"<p><p>We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.</p>","PeriodicalId":7118,"journal":{"name":"Acta geneticae medicae et gemellologiae","volume":"45 1-2","pages":"213-6"},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1017/s000156600000132x","citationCount":"9","resultStr":"{\"title\":\"Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.\",\"authors\":\"D Bettio,&nbsp;D Giardino,&nbsp;N Rizzi,&nbsp;P Riva,&nbsp;L Volpi,&nbsp;E Barantani,&nbsp;A Tagliaferri,&nbsp;L Larizza\",\"doi\":\"10.1017/s000156600000132x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.</p>\",\"PeriodicalId\":7118,\"journal\":{\"name\":\"Acta geneticae medicae et gemellologiae\",\"volume\":\"45 1-2\",\"pages\":\"213-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1996-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1017/s000156600000132x\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta geneticae medicae et gemellologiae\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1017/s000156600000132x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta geneticae medicae et gemellologiae","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1017/s000156600000132x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

摘要

我们报告了一个普雷德-威利综合征(PWS)患者携带平衡的15q15q易位,并受到泌乳素分泌垂体腺瘤的影响。分子研究表明,这种结构重排是母系同工染色体。根据同位体的鉴定作为罕见疾病关联的基础,以及最近关于垂体腺瘤中15号染色体单体和无体的报道,我们认为本例PWS可能与垂体腺瘤有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.

We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信