Indications and management of preimplantation genetic testing for monogenic conditions: a committee opinion

被引:14
|
作者
Penzias, Alan [1 ]
Anderson, Jacob [1 ]
Bendikson, Kristin [1 ]
Gracia, Clarisa [1 ]
Falcone, Tommaso [1 ]
Hansen, Karl [1 ]
Hill, Micah [1 ]
Jin-dal, Sangita [1 ]
Kalra, Suleena [1 ]
Jain, Tarun [1 ]
Thomas, Michael [1 ]
Reindollar, Richard [1 ]
Robins, Jared [1 ]
Shannon, Chevis N. [1 ]
Steiner, Anne [1 ]
Tanrikut, Cigdem [1 ]
Yauger, Belinda [1 ]
Awwad, Rawan [1 ]
Besser, Andria [1 ]
机构
[1] Amer Soc Reprod Med, 1209 Montgomery Highway, Birmingham, AL 35216 USA
关键词
Preimplantation genetic testing; embryo; assisted reproduction; single-gene disorders; IVF; HUNTINGTONS-DISEASE; RECURRENCE RISK; DIAGNOSIS; PGD; DISORDERS; MOSAICISM; PCR;
D O I
10.1016/j.fertnstert.2023.03.003
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
This statement is offered to update and expand on the prior American Society for Reproductive Medicine preimplantation genetic testing (PGT) opinion, elucidate the current clinical and technical complexities specific to PGT for monogenic conditions, assist pro-viders in supporting patient understanding of and access to this technology, and offer considerations for the development of future clinical and laboratory guidelines on PGT for monogenic conditions. (Fertil Steril & REG; 2023;120:61-71. & COPY;2023 by American Society for Reproductive Medicine.)
引用
收藏
页码:61 / 71
页数:11
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