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Responsible implementation of expanded carrier screening

Henneman, L. (author)
Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Sect Community Genet, Amsterdam, Netherlands.;Vrije Univ Amsterdam, Med Ctr, EMGO Inst Hlth & Care Res, Amsterdam, Netherlands.
Borry, P. (author)
Univ Leuven, Ctr Biomed Eth & Law, Leuven, Belgium.,Univ Ljubljana, Med Ctr, Clin Inst Med Genet, Ljubljana 1000, Slovenia.
Chokoshvili, D. (author)
Univ Leuven, Ctr Biomed Eth & Law, Leuven, Belgium.;Univ Hosp Ghent, Ctr Med Genet Ghent, Ghent, Belgium.
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Cornel, M. C. (author)
Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Sect Community Genet, Amsterdam, Netherlands.;Vrije Univ Amsterdam, Med Ctr, EMGO Inst Hlth & Care Res, Amsterdam, Netherlands.
van El, C. G. (author)
Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Sect Community Genet, Amsterdam, Netherlands.;Vrije Univ Amsterdam, Med Ctr, EMGO Inst Hlth & Care Res, Amsterdam, Netherlands.
Forzano, F. (author)
Osped Galliera, Med Genet Unit, Genoa, Italy.
Hall, A. (author)
PHG Fdn, Cambridge, England.
Howard, H. C. (author)
Uppsala universitet,Centrum för forsknings- och bioetik
Janssens, S. (author)
Univ Hosp Ghent, Ctr Med Genet Ghent, Ghent, Belgium.
Kayserili, H. (author)
Koc Univ, Sch Med, Dept Med Genet, Istanbul, Turkey.
Lakeman, P. (author)
Univ Amsterdam, Acad Med Ctr, Dept Clin Genet, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands.
Lucassen, A. (author)
Univ Southampton, Dept Clin Eth & Law CELS, Southampton, Hants, England.;Wessex Clin Genet Serv, Southampton, Hants, England.
Metcalfe, S. A. (author)
Univ Melbourne, Murdoch Childrens Res Inst, Parkville, Vic 3052, Australia.;Univ Melbourne, Dept Paediat, Parkville, Vic 3052, Australia.
Vidmar, L. (author)
Univ Ljubljana, Med Ctr, Clin Inst Med Genet, Ljubljana 1000, Slovenia.
de Wert, G. (author)
Maastricht Univ, Res Sch CAPHRI, Dept Hlth Eth & Soc, NL-6200 MD Maastricht, Netherlands.;Maastricht Univ, Res Sch GROW, NL-6200 MD Maastricht, Netherlands.
Dondorp, W. J. (author)
Maastricht Univ, Res Sch CAPHRI, Dept Hlth Eth & Soc, NL-6200 MD Maastricht, Netherlands.;Maastricht Univ, Res Sch GROW, NL-6200 MD Maastricht, Netherlands.
Peterlin, B. (author)
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Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Sect Community Genet, Amsterdam, Netherlands;Vrije Univ Amsterdam, Med Ctr, EMGO Inst Hlth & Care Res, Amsterdam, Netherlands. Univ Leuven, Ctr Biomed Eth & Law, Leuven, Belgium. (creator_code:org_t)
Springer Science and Business Media LLC, 2016
2016
English.
In: Eur J Hum Genet. - : Springer Science and Business Media LLC. ; 24:6, s. E1-E12
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • This document of the European Society of Human Genetics contains recommendations regarding responsible implementation of expanded carrier screening. Carrier screening is defined here as the detection of carrier status of recessive diseases in couples or persons who do not have an a priori increased risk of being a carrier based on their or their partners' personal or family history. Expanded carrier screening offers carrier screening for multiple autosomal and X-linked recessive disorders, facilitated by new genetic testing technologies, and allows testing of individuals regardless of ancestry or geographic origin. Carrier screening aims to identify couples who have an increased risk of having an affected child in order to facilitate informed reproductive decision making. In previous decades, carrier screening was typically performed for one or few relatively common recessive disorders associated with significant morbidity, reduced life-expectancy and often because of a considerable higher carrier frequency in a specific population for certain diseases. New genetic testing technologies enable the expansion of screening to multiple conditions, genes or sequence variants. Expanded carrier screening panels that have been introduced to date have been advertised and offered to health care professionals and the public on a commercial basis. This document discusses the challenges that expanded carrier screening might pose in the context of the lessons learnt from decades of population-based carrier screening and in the context of existing screening criteria. It aims to contribute to the public and professional discussion and to arrive at better clinical and laboratory practice guidelines.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Medicinsk etik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Medical Ethics (hsv//eng)

Keyword

Decision Making
Europe
Genetic Counseling/ethics/*psychology
Genetic Testing/ethics/*standards
Genetics
Medical/ethics/organization & administration
*Heterozygote
Humans
*Practice Guidelines as Topic
Societies
Medical
Bioetik
Bioethics

Publication and Content Type

ref (subject category)
art (subject category)

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