Predictors of poor prognosis in preimplantation genetic testing for monogenic disorders (PGT-M)

被引:0
|
作者
Verpoest, W. [1 ]
Verdyck, P. [2 ]
De Vos, A. [1 ]
De Rycke, M. [2 ]
Liebaers, I. [2 ]
Blockeel, C. [1 ]
Berckmoes, V. [2 ]
De Becker, P. [2 ]
De Vos, M. [1 ]
Keymolen, K. [2 ]
Santos-Ribeiro, S. [1 ]
机构
[1] UZ Brussel, Ctr Reprod Med, Jette Brussels, Belgium
[2] UZ Brussel, Ctr Med Genet, Jette Brussels, Belgium
关键词
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
O-079
引用
收藏
页码:36 / 36
页数:1
相关论文
共 50 条
  • [41] The effect of repeated biopsy on pre-implantation genetic testing for monogenic diseases (PGT-M) treatment outcome
    Shira Priner
    Gheona Altarescu
    Oshrat Schonberger
    Hananel Holzer
    Esther Rubinstein
    Nava Dekel
    Aharon Peretz
    Talia Eldar-Geva
    [J]. Journal of Assisted Reproduction and Genetics, 2019, 36 : 159 - 164
  • [42] The effect of repeated biopsy on pre-implantation genetic testing for monogenic diseases (PGT-M) treatment outcome
    Priner, Shira
    Altarescu, Gheona
    Schonberger, Oshrat
    Holzer, Hananel
    Rubinstein, Esther
    Dekel, Nava
    Peretz, Aharon
    Eldar-Geva, Talia
    [J]. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2019, 36 (01) : 159 - 164
  • [43] Preimplantation genetic testing for monogenic disease (PGT-M) where results are only based upon analysis of linked polymorphisms/haplotypes risks serious diagnostic errors
    Ali, A. Haj
    Ampiah, M.
    Abdous, H.
    Babariya, D.
    Raberi, A.
    Wells, D.
    [J]. HUMAN REPRODUCTION, 2023, 38
  • [44] Preimplantation genetic testing (PGT-M) for Parkinson disease (PD) risk reduction: Expanding of applications for selecting embryos
    Zuckerman, Shachar
    Zimran, Ari
    Eldar-Geva, Talya
    Farhi, Elina
    Shaviv, Shira
    Hakam-Spector, Elinor
    Dinur, Tama
    Altarescu, Gheona
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 107 - 107
  • [45] Psychological burden of preimplantation genetic testing (PGT) on mothers with multiple monogenic disorders and the role of genetic counselling in Saudi Arabia
    AlShehri, Monira
    Qari, Alya
    AlSayed, Moeenaldeen
    Balobaid, Ameera
    AlQubbaj, Wafa
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 566 - 566
  • [46] Examining the success rates following a second embryo biopsy for inconclusive results in preimplantation genetic testing for monogenic diseases (PGT-M): a matched case-control study
    Perego, L.
    Sanzani, E.
    Ciaffaglione, M.
    Levi, S. L.
    Tondo, F.
    Riccaboni, A.
    Somigliana, E.
    [J]. HUMAN REPRODUCTION, 2024, 39 : I429 - I429
  • [47] BENEFIT OF BROADENED SCREENING OF X-LINKED DISEASES (XLD): REFERRAL TRENDS TO PREIMPLANTATION GENETIC TESTING (PGT-M).
    Morris, J. M.
    Bristow, S. L.
    Jordan, A.
    Armenti, E.
    Nisson, H.
    Hershlag, A.
    [J]. FERTILITY AND STERILITY, 2018, 110 (04) : E146 - E146
  • [48] PGT-M TO PREVENT 2 OR 3 GENETIC DISORDERS, MOSTLY DOMINANT.
    Peyser, Alexandra
    McWilliams, Kristine
    Hershlag, Avner
    [J]. FERTILITY AND STERILITY, 2021, 116 (03) : E396 - E396
  • [49] The impact of a second embryo biopsy for preimplantation genetic testing for monogenic diseases (PGT-M) with inconclusive results on pregnancy potential: results from a matched case-control study
    Guarneri, Cristina
    Reschini, Marco
    Pinna, Monica
    Perego, Lucia
    Sanzani, Elena
    Somigliana, Edgardo
    Sorrentino, Ugo
    Cassina, Matteo
    Zuccarello, Daniela
    Ciaffaglione, Marta
    [J]. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2024, 41 (06) : 1605 - 1617
  • [50] Preimplantation genetic testing for monogenic disorders (PGT-M) offers an alternative strategy to prevent children from being born with hereditary neurological diseases or metabolic diseases dominated by nervous system phenotypes: a retrospective study
    Zou, Weiwei
    Li, Min
    Wang, Xiaolei
    Lu, Hedong
    Hao, Yan
    Chen, Dawei
    Zhu, Shasha
    Ji, Dongmei
    Zhang, Zhiguo
    Zhou, Ping
    Cao, Yunxia
    [J]. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2024, 41 (05) : 1245 - 1259