Genetisk screening af adopterede raske individer
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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Genetisk screening af adopterede raske individer. / Wriedt, Tanja Røhmer; Gerdes, Anne-Marie Axø; Roos, Laura Kristine; Hammer-Hansen, Sophia; Christensen, Maja Bejerholm; Diness, Birgitte Rode.
I: Ugeskrift for Laeger, Bind 183, Nr. 13, V11200810, 29.03.2021.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Genetisk screening af adopterede raske individer
AU - Wriedt, Tanja Røhmer
AU - Gerdes, Anne-Marie Axø
AU - Roos, Laura Kristine
AU - Hammer-Hansen, Sophia
AU - Christensen, Maja Bejerholm
AU - Diness, Birgitte Rode
PY - 2021/3/29
Y1 - 2021/3/29
N2 - Information regarding hereditary disease predisposition is generally inaccessible for adoptees. The lack of family history restricts access to various surveillance programmes and the overall health of the adoptee. Genetic screening of asymptomatic adoptees could be a compensational tool. However, variant classification is difficult, even more so in certain ethnic groups and in cases where there is no knowledge of family history, as summarised in this review. The usefulness of genetic screening of asymptomatic adoptees is still unknown and requires further research for clarification.
AB - Information regarding hereditary disease predisposition is generally inaccessible for adoptees. The lack of family history restricts access to various surveillance programmes and the overall health of the adoptee. Genetic screening of asymptomatic adoptees could be a compensational tool. However, variant classification is difficult, even more so in certain ethnic groups and in cases where there is no knowledge of family history, as summarised in this review. The usefulness of genetic screening of asymptomatic adoptees is still unknown and requires further research for clarification.
KW - Adoption
KW - Genetic Predisposition to Disease
KW - Genetic Testing
KW - Humans
KW - Medical History Taking
M3 - Tidsskriftartikel
C2 - 33829992
VL - 183
JO - Ugeskrift for Laeger
JF - Ugeskrift for Laeger
SN - 0041-5782
IS - 13
M1 - V11200810
ER -
ID: 305553156