"i do not want my baby to suffer as i did"; Prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: A case report and genetic counseling considerations

Efrat Dagan; Ruth Gershoni-Baruch; Alina Kurolap; Yael Goldberg; Georgeta Fried

doi:10.1089/gtmb.2013.0513

"i do not want my baby to suffer as i did"; Prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: A case report and genetic counseling considerations

Efrat Dagan, Ruth Gershoni-Baruch, Alina Kurolap, Yael Goldberg, Georgeta Fried

University of Haifa, Technion - Israel Institute of Technology

Research output: Contribution to journal › Review article › peer-review

Abstract

This article presents the complexity of prenatal genetic diagnosis and preimplantation genetic diagnosis for hereditary breast-ovarian cancer syndrome. These issues are discussed using a case report to highlight the genetic counseling process, together with decision-making considerations, in light of the clinical, psychological, and ethical perspectives, of both the mutation carriers and health professionals; and the health policy regarding these procedures in Israel compared to several European countries.

Original language	American English
Pages (from-to)	461-466
Number of pages	6
Journal	Genetic Testing and Molecular Biomarkers
Volume	18
Issue number	7
DOIs	https://doi.org/10.1089/gtmb.2013.0513
State	Published - 1 Jul 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

Genetics(clinical)

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10.1089/gtmb.2013.0513

Cite this

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"i do not want my baby to suffer as i did"; Prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: A case report and genetic counseling considerations. / Dagan, Efrat; Gershoni-Baruch, Ruth; Kurolap, Alina et al.
In: Genetic Testing and Molecular Biomarkers, Vol. 18, No. 7, 01.07.2014, p. 461-466.

Research output: Contribution to journal › Review article › peer-review

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AU - Gershoni-Baruch, Ruth

AU - Kurolap, Alina

AU - Goldberg, Yael

AU - Fried, Georgeta

PY - 2014/7/1

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N2 - This article presents the complexity of prenatal genetic diagnosis and preimplantation genetic diagnosis for hereditary breast-ovarian cancer syndrome. These issues are discussed using a case report to highlight the genetic counseling process, together with decision-making considerations, in light of the clinical, psychological, and ethical perspectives, of both the mutation carriers and health professionals; and the health policy regarding these procedures in Israel compared to several European countries.

AB - This article presents the complexity of prenatal genetic diagnosis and preimplantation genetic diagnosis for hereditary breast-ovarian cancer syndrome. These issues are discussed using a case report to highlight the genetic counseling process, together with decision-making considerations, in light of the clinical, psychological, and ethical perspectives, of both the mutation carriers and health professionals; and the health policy regarding these procedures in Israel compared to several European countries.

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JO - Genetic Testing and Molecular Biomarkers

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"i do not want my baby to suffer as i did"; Prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: A case report and genetic counseling considerations

Abstract

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