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With expanded carrier screening, founder populations run the risk of being overlooked
Genetically isolated populations exist worldwide. Specific genetic disorders, including rare autosomal recessive disorders may have high prevalences in these populations. We searched for Dutch genetically isolated populations and their autosomal recessive founder mutations. We investigated whether t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614881/ https://www.ncbi.nlm.nih.gov/pubmed/28555434 http://dx.doi.org/10.1007/s12687-017-0309-5 |
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author | Mathijssen, Inge B. van Maarle, Merel C. Kleiss, Iris I.M. Redeker, Egbert J.W. ten Kate, Leo P. Henneman, Lidewij Meijers-Heijboer, Hanne |
author_facet | Mathijssen, Inge B. van Maarle, Merel C. Kleiss, Iris I.M. Redeker, Egbert J.W. ten Kate, Leo P. Henneman, Lidewij Meijers-Heijboer, Hanne |
author_sort | Mathijssen, Inge B. |
collection | PubMed |
description | Genetically isolated populations exist worldwide. Specific genetic disorders, including rare autosomal recessive disorders may have high prevalences in these populations. We searched for Dutch genetically isolated populations and their autosomal recessive founder mutations. We investigated whether these founder mutations are covered in the (preconception) expanded carrier screening tests of five carrier screening providers. Our results show that the great majority of founder mutations are not covered in these screening panels, and these panels may thus not be appropriate for use in founder populations. It is therefore important to be aware of founder mutations in a population when offering carrier tests. |
format | Online Article Text |
id | pubmed-5614881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-56148812017-10-11 With expanded carrier screening, founder populations run the risk of being overlooked Mathijssen, Inge B. van Maarle, Merel C. Kleiss, Iris I.M. Redeker, Egbert J.W. ten Kate, Leo P. Henneman, Lidewij Meijers-Heijboer, Hanne J Community Genet Original Article Genetically isolated populations exist worldwide. Specific genetic disorders, including rare autosomal recessive disorders may have high prevalences in these populations. We searched for Dutch genetically isolated populations and their autosomal recessive founder mutations. We investigated whether these founder mutations are covered in the (preconception) expanded carrier screening tests of five carrier screening providers. Our results show that the great majority of founder mutations are not covered in these screening panels, and these panels may thus not be appropriate for use in founder populations. It is therefore important to be aware of founder mutations in a population when offering carrier tests. Springer Berlin Heidelberg 2017-05-29 2017-10 /pmc/articles/PMC5614881/ /pubmed/28555434 http://dx.doi.org/10.1007/s12687-017-0309-5 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Mathijssen, Inge B. van Maarle, Merel C. Kleiss, Iris I.M. Redeker, Egbert J.W. ten Kate, Leo P. Henneman, Lidewij Meijers-Heijboer, Hanne With expanded carrier screening, founder populations run the risk of being overlooked |
title | With expanded carrier screening, founder populations run the risk of being overlooked |
title_full | With expanded carrier screening, founder populations run the risk of being overlooked |
title_fullStr | With expanded carrier screening, founder populations run the risk of being overlooked |
title_full_unstemmed | With expanded carrier screening, founder populations run the risk of being overlooked |
title_short | With expanded carrier screening, founder populations run the risk of being overlooked |
title_sort | with expanded carrier screening, founder populations run the risk of being overlooked |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614881/ https://www.ncbi.nlm.nih.gov/pubmed/28555434 http://dx.doi.org/10.1007/s12687-017-0309-5 |
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