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本文引用的文献

1
Quality of life and psychological distress in patients with Peutz-Jeghers syndrome.患 Peutz-Jeghers 综合征患者的生活质量和心理困扰。
Clin Genet. 2010 Sep;78(3):219-26. doi: 10.1111/j.1399-0004.2010.01469.x.
2
High cancer risk in Peutz-Jeghers syndrome: a systematic review and surveillance recommendations.Peutz-Jeghers 综合征的高癌症风险:系统评价和监测建议。
Am J Gastroenterol. 2010 Jun;105(6):1258-64; author reply 1265. doi: 10.1038/ajg.2009.725. Epub 2010 Jan 5.
3
Perspectives of couples with high risk of transmitting genetic disorders.具有遗传疾病高传播风险的夫妇的观点。
Fertil Steril. 2010 Sep;94(4):1239-1243. doi: 10.1016/j.fertnstert.2009.08.025. Epub 2009 Oct 7.
4
Attitudes toward genetic testing in childhood and reproductive decision-making for familial adenomatous polyposis.儿童期遗传检测态度与家族性腺瘤性息肉病的生殖决策。
Eur J Hum Genet. 2010 Feb;18(2):186-93. doi: 10.1038/ejhg.2009.151. Epub 2009 Oct 7.
5
Attitude towards pre-implantation genetic diagnosis for hereditary cancer.遗传性癌症的胚胎植入前遗传学诊断的态度。
Fam Cancer. 2009;8(4):457-64. doi: 10.1007/s10689-009-9265-5. Epub 2009 Jul 30.
6
Psychosocial impact of Peutz-Jeghers Syndrome.黑斑息肉综合征的社会心理影响。
Fam Cancer. 2009;8(1):59-65. doi: 10.1007/s10689-008-9202-z. Epub 2008 Jul 5.
7
Views of BRCA gene mutation carriers on preimplantation genetic diagnosis as a reproductive option for hereditary breast and ovarian cancer.BRCA基因突变携带者对胚胎植入前遗传学诊断作为遗传性乳腺癌和卵巢癌生殖选择的看法。
Hum Reprod. 2007 Jun;22(6):1573-7. doi: 10.1093/humrep/dem055. Epub 2007 Apr 11.
8
Attitudes toward prenatal genetic testing in patients with familial adenomatous polyposis.家族性腺瘤性息肉病患者对产前基因检测的态度。
Am J Gastroenterol. 2007 Jun;102(6):1284-90. doi: 10.1111/j.1572-0241.2007.01168.x. Epub 2007 Mar 13.
9
Clinical practice. In vitro fertilization.临床实践。体外受精。
N Engl J Med. 2007 Jan 25;356(4):379-86. doi: 10.1056/NEJMcp065743.
10
Peutz-Jeghers syndrome: clinicopathology and molecular alterations.佩-吉二氏综合征:临床病理学与分子改变
Cell Mol Life Sci. 2006 Sep;63(18):2135-44. doi: 10.1007/s00018-006-6080-0.

佩吉特-杰格斯综合征与计划生育:对产前诊断和胚胎植入前遗传学诊断的态度。

Peutz-Jeghers syndrome and family planning: the attitude towards prenatal diagnosis and pre-implantation genetic diagnosis.

机构信息

Departments of Gastroenterology and Hepatology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

出版信息

Eur J Hum Genet. 2012 Feb;20(2):236-9. doi: 10.1038/ejhg.2011.152. Epub 2011 Aug 10.

DOI:10.1038/ejhg.2011.152
PMID:21829227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3260925/
Abstract

Peutz-Jeghers syndrome (PJS) is a hereditary disorder caused by LKB1 gene mutations, and is associated with considerable morbidity and decreased life expectancy. This study was conducted to assess the attitude of PJS patients towards family planning, prenatal diagnosis (PND) and pregnancy termination, and pre-implantation genetic diagnosis (PGD). In a cross-sectional study, 61 adult PJS patients were asked to complete a questionnaire concerning genetic testing, family planning, PND and PGD. The questionnaire was completed by 52 patients (85% response rate, 44% males) with a median age of 44 (range 18-74) years. A total of 37 (71%) respondents had undergone genetic testing. In all, 24 respondents (46%, 75% males) had children. A total of 15 (29%) respondents reported that their diagnosis of PJS had influenced their decisions regarding family planning, including 10 patients (19%, 9/10 females) who did not want to have children because of their disease. Termination of pregnancy after PND in case of a foetus with PJS was considered 'acceptable' for 15% of the respondents, whereas 52% considered PGD acceptable. In conclusion, the diagnosis of PJS influences the decisions regarding family planning in one third of PJS patients, especially in women. Most patients have a negative attitude towards pregnancy termination after PND, while PGD in case of PJS is judged more acceptable. These results emphasise the importance of discussing aspects regarding family planning with PJS patients, including PND and PGD.

摘要

佩吉特-杰格斯综合征(PJS)是一种由 LKB1 基因突变引起的遗传性疾病,与相当高的发病率和预期寿命降低有关。本研究旨在评估 PJS 患者对计划生育、产前诊断(PND)和终止妊娠以及植入前遗传学诊断(PGD)的态度。在一项横断面研究中,我们要求 61 名成年 PJS 患者填写一份关于基因检测、计划生育、PND 和 PGD 的问卷。共有 52 名患者(85%的应答率,44%为男性)完成了问卷,中位年龄为 44 岁(范围 18-74 岁)。共有 37 名(71%)患者接受了基因检测。共有 24 名(46%,75%为男性)患者有子女。共有 15 名(29%)患者表示,他们的 PJS 诊断影响了他们对计划生育的决定,包括 10 名患者(19%,10/10 为女性)因疾病而不想生育。15%的患者认为 PND 后终止妊娠(如果胎儿患有 PJS)是“可接受的”,而 52%的患者认为 PGD 是可接受的。总之,三分之一的 PJS 患者的 PJS 诊断会影响他们的计划生育决定,尤其是女性。大多数患者对 PND 后终止妊娠持否定态度,而对 PJS 患者的 PGD 则持更为认可的态度。这些结果强调了与 PJS 患者讨论计划生育方面的重要性,包括 PND 和 PGD。