Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoa
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2833375
Author(s) De Geyter, Christian; Sterthaus, Oliver; Miny, Peter; Wenzel, Friedel; Lapaire, Olav; De Geyter, Maria; Sartorius, Gideon
Author(s) at UniBasel de Geyter, Christian M.H.R.
Year 2013
Title First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoa
Journal Swiss medical weekly
Volume 143
Pages / Article-Number w13718
Keywords preimplantation genetic diagnosis, assisted reproduction, flow cytometry, semen preparation, X-linked disorders
Abstract QUESTION UNDER STUDY: The feasibility and the potential advantages of separating X-chromosome bearing spermatozoa for the prevention of a severe X-chromosome linked disorder with the use of intracytoplasmic sperm injection are presented. METHOD: A carrier of muscular dystrophy type Becker was treated with intracytoplasmic sperm injection, using spermatozoa previously stained with the Hoechst dye 33342 and sorted with flow cytometry. RESULTS: After transfer of one single blastocyst, an intrauterine pregnancy arose. In the ninth week of gestation, the female sex of the embryo was confirmed with proof of absence of the SRY gene of the Y-chromosome. After normal pregnancy, the patient delivered a healthy daughter. CONCLUSIONS: The staining of spermatozoa with specific markers and sorting with flow cytometry provides a means of preventing significant disease in the offspring and may help in reducing the number of surplus embryos needed for preimplantation genetic diagnosis.
Publisher EMH
ISSN/ISBN 1424-7860
edoc-URL http://edoc.unibas.ch/dok/A6338666
Full Text on edoc No
Digital Object Identifier DOI 10.4414/smw.2013.13718
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/23444294
ISI-Number WOS:000321908400001
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.369 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
07/05/2024