Preimplantation genetic testing as a component of root cause analysis of errors and reassignment of embryos in IVF

被引：2

作者：

Bunnell, Megan ^{[1
]}

Esfandiari, Navid ^{[2
]}

机构：

[1] Brigham & Womens Hosp, Dept Obstet & Gynecol, 75 Francis St, Boston, MA 02115 USA

[2] Univ Vermont, Larner Coll Med, Med Ctr, Dept Obstet & Gynecol & Reprod Sci, Burlington, VT 05405 USA

来源：

REPRODUCTIVE BIOMEDICINE ONLINE | 2020年 / 41卷 / 06期

关键词：

Embryo biopsy; IVF errors; Paternity testing; Preimplantation genetic testing; Single-nucleotide polymorphism; TECHNOLOGIES;

D O I：

10.1016/j.rbmo.2020.08.031

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

The risks of embryo/gamete mix-up are a threat to the integrity of the IVF process, with significant implications for affected families. The use of preimplantation genetic testing through single-nucleotide polymorphism array or next generation sequencing technology can help to identify, characterize and ultimately help, in some cases, to find the root cause, and to mitigate the extent of these errors for a given patient or laboratory.

引用

页码：975 / 977

页数：3

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