Det danske screeningsprogram for hæmoglobinopatier

Andreas Glenthøj; Mie Samson; Nina Toft; Birgitte Rode Diness; Nikolaj Askj R; Fie Juhl Vojdeman; Henrik Birgens; Morten Beck Sørensen; Jesper Petersen

Det danske screeningsprogram for hæmoglobinopatier

Andreas Glenthøj, Mie Samson, Nina Toft, Birgitte Rode Diness, Nikolaj Askj R, Fie Juhl Vojdeman, Henrik Birgens, Morten Beck Sørensen, Jesper Petersen

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

2 Citationer (Scopus)

9 Downloads (Pure)

Abstract

The prevalence of people in Denmark descending from areas with a high prevalence of haemoglobinopathies is approximately one tenth and increasing. Since 1995, the Danish Health Authority has recommended haemoglobinopathy screening of pregnant women with ethnic roots outside Northern Europe. Partners of pregnant haemoglobinopathy carriers are also tested. Carrier state in both parents leads to genetic counselling, and prenatal diagnostics of the foetus (chorionic villus biopsy or amniocentesis) is offered, which can lead to abortion and/or preimplantation genetic screening for future pregnancies, as discussed in this review.

Bidragets oversatte titel	The Danish screening programme for haemoglobinopathies
Originalsprog	Dansk
Artikelnummer	V07200536
Tidsskrift	Ugeskrift for Laeger
Vol/bind	183
Udgave nummer	3
Antal sider	8
ISSN	0041-5782
Status	Udgivet - 18 jan. 2021

Emneord

Amniocentesis
Denmark/epidemiology
Europe
Female
Hemoglobinopathies/diagnosis
Humans
Pregnancy
Prenatal Diagnosis

Adgang til dokumentet

FulltextForlagets udgivne version, 453 KBLicens: CC BY-NC-ND

https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2021-01/v07200536_web.pdf

Citationsformater

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abstract = "The prevalence of people in Denmark descending from areas with a high prevalence of haemoglobinopathies is approximately one tenth and increasing. Since 1995, the Danish Health Authority has recommended haemoglobinopathy screening of pregnant women with ethnic roots outside Northern Europe. Partners of pregnant haemoglobinopathy carriers are also tested. Carrier state in both parents leads to genetic counselling, and prenatal diagnostics of the foetus (chorionic villus biopsy or amniocentesis) is offered, which can lead to abortion and/or preimplantation genetic screening for future pregnancies, as discussed in this review.",

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T1 - Det danske screeningsprogram for hæmoglobinopatier

AU - Glenthøj, Andreas

AU - Samson, Mie

AU - Toft, Nina

AU - Diness, Birgitte Rode

AU - Askj R, Nikolaj

AU - Vojdeman, Fie Juhl

AU - Birgens, Henrik

AU - Sørensen, Morten Beck

AU - Petersen, Jesper

PY - 2021/1/18

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N2 - The prevalence of people in Denmark descending from areas with a high prevalence of haemoglobinopathies is approximately one tenth and increasing. Since 1995, the Danish Health Authority has recommended haemoglobinopathy screening of pregnant women with ethnic roots outside Northern Europe. Partners of pregnant haemoglobinopathy carriers are also tested. Carrier state in both parents leads to genetic counselling, and prenatal diagnostics of the foetus (chorionic villus biopsy or amniocentesis) is offered, which can lead to abortion and/or preimplantation genetic screening for future pregnancies, as discussed in this review.

AB - The prevalence of people in Denmark descending from areas with a high prevalence of haemoglobinopathies is approximately one tenth and increasing. Since 1995, the Danish Health Authority has recommended haemoglobinopathy screening of pregnant women with ethnic roots outside Northern Europe. Partners of pregnant haemoglobinopathy carriers are also tested. Carrier state in both parents leads to genetic counselling, and prenatal diagnostics of the foetus (chorionic villus biopsy or amniocentesis) is offered, which can lead to abortion and/or preimplantation genetic screening for future pregnancies, as discussed in this review.

KW - Amniocentesis

KW - Denmark/epidemiology

KW - Europe

KW - Female

KW - Hemoglobinopathies/diagnosis

KW - Humans

KW - Pregnancy

KW - Prenatal Diagnosis

M3 - Tidsskriftartikel

C2 - 33491643

SN - 0041-5782

VL - 183

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

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