H Dechaud (Maître de conférences des Universités, praticien hospitalier) , T Anahory (Praticien hospitalier) , A Girardet (Docteur es Science) , C Coubes (Praticien hospitalier) , V Cacheux (Maître de conférences des Universités, praticien hospitalier) , S Hamamah (Professeur des Universités, praticien hospitalier) , M Claustres (Professeur des Universités, praticien hospitalier)
{"title":"Diagnostic pré-implantatoire","authors":"H Dechaud (Maître de conférences des Universités, praticien hospitalier) , T Anahory (Praticien hospitalier) , A Girardet (Docteur es Science) , C Coubes (Praticien hospitalier) , V Cacheux (Maître de conférences des Universités, praticien hospitalier) , S Hamamah (Professeur des Universités, praticien hospitalier) , M Claustres (Professeur des Universités, praticien hospitalier)","doi":"10.1016/j.emcgo.2004.02.002","DOIUrl":null,"url":null,"abstract":"<div><p>Fourteen years ago, the first preimplantation genetic diagnosis was described in the literature. The aim of the preimplantation genetic diagnosis is to analyse genes or chromosomes of embryos just before their transfer into the uterus. This technique avoids, for an identified pathology, the birth of children suffering from this pathology or repetitive medical abortions after prenatal diagnosis. The preimplantation genetic diagnosis needs to be performed by a multidisciplinary team working in well defined legal conditions. The preimplantation genetic diagnosis procedure includes an in vitro fertilization and intracytoplasmic sperm injection, a biopsy of one embryo cell and the genetic analysis of this cell. However, only a restricted number of genetic pathologies can benefit from such management. Preimplantation genetic diagnosis is a promising procedure for numerous patients. However, the evolution of its indications highlights the importance of informing both the couples and the society.</p></div>","PeriodicalId":100424,"journal":{"name":"EMC - Gynécologie-Obstétrique","volume":"1 2","pages":"Pages 76-87"},"PeriodicalIF":0.0000,"publicationDate":"2004-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.emcgo.2004.02.002","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EMC - Gynécologie-Obstétrique","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1762614504000095","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Fourteen years ago, the first preimplantation genetic diagnosis was described in the literature. The aim of the preimplantation genetic diagnosis is to analyse genes or chromosomes of embryos just before their transfer into the uterus. This technique avoids, for an identified pathology, the birth of children suffering from this pathology or repetitive medical abortions after prenatal diagnosis. The preimplantation genetic diagnosis needs to be performed by a multidisciplinary team working in well defined legal conditions. The preimplantation genetic diagnosis procedure includes an in vitro fertilization and intracytoplasmic sperm injection, a biopsy of one embryo cell and the genetic analysis of this cell. However, only a restricted number of genetic pathologies can benefit from such management. Preimplantation genetic diagnosis is a promising procedure for numerous patients. However, the evolution of its indications highlights the importance of informing both the couples and the society.
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