Association of non-invasive prenatal testing and chromosomal microarray analysis for prenatal diagnostics

The purposes of this study is to examine possibility to use combination of non-invasive prenatal testing (NIPT) and chromosomal microarray analysis (CMA) for prenatal diagnostics and their advantages between combined first-trimester screen with confirmation by karyotyping of CVS or amniocytes. A total of 1968 pregnant women, in this study, have undergone prenatal screening and/or diagnostic tests. NIPT is more suitable and efficient for the detection of aneuploidy. However, this test has limitations for detection deletions/duplications. Use of CMA for confirmation of some NIPT findings or as first test for women with ultrasound abnormalities can detect small imbalances in chromosomes. Combination of NIPT and CMA allows a higher prenatal detection of chromosomal abnormalities. © 2014 Informa UK Ltd.

Авторы
Korostelev S.1 , Totchiev G. 2 , Kanivets I.3 , Gnetetskaya V.4
Язык
Английский
Страницы
13-16
Статус
Опубликовано
Том
30
Год
2014
Организации
  • 1 First Moscow Medical University, Moscow, Russian Federation
  • 2 Peoples' Friendship University of Russia, Moscow, Russian Federation
  • 3 Filatov's Child Hospital, Moscow, Russian Federation
  • 4 Mother and Child Clinic, Moscow, Russian Federation
Ключевые слова
Chromosomal microarray analysis; Non-invasive prenatal test; Prenatal diagnostics
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/4980/
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