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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.
Afiliação
  • Mathijssen IB; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands. i.b.mathijssen@amc.uva.nl.
  • van Maarle MC; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Kleiss IIM; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Redeker EJW; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Ten Kate LP; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Henneman L; Amsterdam Public Health Research Institute, VU University Medical Center, Amsterdam, The Netherlands.
  • Meijers-Heijboer H; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
J Community Genet ; 8(4): 327-333, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28555434
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: J Community Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: J Community Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda