dc.contributor.author | Tanacan, Atakan | |
dc.contributor.author | Unal, Canan | |
dc.contributor.author | Yucesoy, Halise Meltem | |
dc.contributor.author | Fadiloglu, Erdem | |
dc.contributor.author | Beksac, M. Sinan | |
dc.date.accessioned | 2021-06-03T06:15:47Z | |
dc.date.available | 2021-06-03T06:15:47Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 0972-3757 | |
dc.identifier.uri | http://dx.doi.org/10.31901/24566330.2019/19.03.723 | |
dc.identifier.uri | http://hdl.handle.net/11655/24260 | |
dc.description.abstract | The researchers retrospectively evaluated the data of patients who underwent invasive prenatal diagnostic tests with respect to the following risk factors: 1) history of chromosomal abnormality in the family (n=36), 2) history of chromosomal abnormality in a previous pregnancy (n=18), and 3) history of chromosomal abnormality in the parents (n=3) between 2000 and 2017. The diagnostic test results of patients with a history of chromosomal abnormality in the family and those with a history of a chromosomal abnormality in a previous pregnancy were compared. A total of 57 invasive procedures were evaluated. The aneuploidy rates were 41.7 percent and 16.7 percent for patients with a history of chromosomal abnormality in the family and patients with a history of chromosomal abnormality in a previous pregnancy respectively (p = 0.085). Invasive prenatal tests should be recommended to patients at high risk of chromosomal aneuploidy. | |
dc.language.iso | en | |
dc.relation.isversionof | 10.31901/24566330.2019/19.03.723 | |
dc.rights | Attribution 4.0 United States | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Amniocentesis | |
dc.subject | Chordocentesi | |
dc.subject | Chorion Villus Sampling | |
dc.subject | High Risk Pregnancy | |
dc.title | Importance Of Prenatal Diagnosis In Patients With History Of Chromosomal Abnormalities | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:eu-repo/semantics/publishedVersion | |
dc.relation.journal | International Journal Of Human Genetics | |
dc.contributor.department | Kadın Hastalıkları ve Doğum | |
dc.identifier.volume | 19 | |
dc.identifier.issue | 3 | |
dc.description.index | WoS | |