Literature DB >> 19155287

The causes of misdiagnosis and adverse outcomes in PGD.

L Wilton1, A Thornhill, J Traeger-Synodinos, K D Sermon, J C Harper.   

Abstract

The European Society of Human Reproduction and Embryology PGD Consortium has collected data on PGD cycles and deliveries since 1997. From 15,158 cycles, 24 misdiagnoses and adverse outcomes have been reported; 12/2538 cycles after polymerase chain reaction and 12/12,620 cycles after fluorescence in situ hybridization. The causes of misdiagnosis include confusion of embryo and cell number, transfer of the wrong embryo, maternal or paternal contamination, allele dropout, use of incorrect and inappropriate probes or primers, probe or primer failure and chromosomal mosaicism. Unprotected sex has been mentioned as a cause of adverse outcome not related to technical and human errors. The majority of these causes can be prevented by using robust diagnostic methods within laboratories working to appropriate quality standards. However, diagnosis from a single cell remains a technically challenging procedure, and the risk of misdiagnosis cannot be eliminated.

Entities:  

Mesh:

Year:  2009        PMID: 19155287     DOI: 10.1093/humrep/den488

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  49 in total

1.  Singling out genetic disorders and disease.

Authors:  Martine De Rycke
Journal:  Genome Med       Date:  2010-10-06       Impact factor: 11.117

2.  Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.

Authors:  Maartje C Van Rij; Marjan De Rademaeker; Céline Moutou; Jos C F M Dreesen; Martine De Rycke; Inge Liebaers; Joep P M Geraedts; Christine E M De Die-Smulders; Stéphane Viville
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

3.  The clinical application of preimplantation genetic diagnosis for the patient affected by congenital contractural arachnodactyly and spinal and bulbar muscular atrophy.

Authors:  Linjun Chen; Zhenyu Diao; Zhipeng Xu; Jianjun Zhou; Wanjun Wang; Jie Li; Guijun Yan; Haixiang Sun
Journal:  J Assist Reprod Genet       Date:  2016-07-09       Impact factor: 3.412

4.  Familial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle study.

Authors:  G Altarescu; D A Zeevi; S Zeligson; S Perlberg; T Eldar-Geva; E J Margalioth; E Levy-Lahad; P Renbaum
Journal:  J Assist Reprod Genet       Date:  2013-07-06       Impact factor: 3.412

5.  Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study.

Authors:  Jos Dreesen; Aspasia Destouni; Georgia Kourlaba; Birte Degn; Wulf Christensen Mette; Filipa Carvalho; Celine Moutou; Sioban Sengupta; Seema Dhanjal; Pamela Renwick; Steven Davies; Emmanouel Kanavakis; Gary Harton; Joanne Traeger-Synodinos
Journal:  Eur J Hum Genet       Date:  2013-12-04       Impact factor: 4.246

6.  Pregnancy after PGD for recessive dystrophic epidermolysis bullosa inversa: genetics and preimplantation genetics.

Authors:  Xavier Vendrell; Rosa Bautista-Llácer; Trinitat Maria Alberola; Elena García-Mengual; Merche Pardo; Antonio Urries; Julián Sánchez
Journal:  J Assist Reprod Genet       Date:  2011-06-24       Impact factor: 3.412

Review 7.  PGS-FISH in reproductive medicine and perspective directions for improvement: a systematic review.

Authors:  Sandra Zamora; Ana Clavero; M Carmen Gonzalvo; Juan de Dios Luna Del Castillo; Jose Antonio Roldán-Nofuentes; Juan Mozas; Jose Antonio Castilla
Journal:  J Assist Reprod Genet       Date:  2011-06-29       Impact factor: 3.412

8.  Outcomes of medical malpractice claims in assisted reproductive technology over a 10-year period from a single carrier.

Authors:  Gerard Letterie
Journal:  J Assist Reprod Genet       Date:  2017-02-11       Impact factor: 3.412

9.  Genotyping single-sperm cells by universal MARSALA enables the acquisition of linkage information for combined pre-implantation genetic diagnosis and genome screening.

Authors:  Haitao Wu; Xiaoting Shen; Lei Huang; Yanhong Zeng; Yumei Gao; Lin Shao; Baomin Lu; Yiping Zhong; Benyu Miao; Yanwen Xu; Yali Wang; Yubin Li; Luoxing Xiong; Sijia Lu; X Sunney Xie; Canquan Zhou
Journal:  J Assist Reprod Genet       Date:  2018-05-22       Impact factor: 3.412

10.  Replication independent DNA double-strand break retention may prevent genomic instability.

Authors:  Narisorn Kongruttanachok; Chutipa Phuangphairoj; Araya Thongnak; Wanpen Ponyeam; Prakasit Rattanatanyong; Wichai Pornthanakasem; Apiwat Mutirangura
Journal:  Mol Cancer       Date:  2010-03-31       Impact factor: 27.401

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