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Screening for fragilt X-syndrom. Internationale erfaringer
Engelsk titel: Screening for fragile X syndrome. International experiences Läs online Författare: Vuust J ; Larsen LA ; Grönskov K ; Nörgaard-Pedersen B ; Bröndum-Nielsen K Språk: Dan Antal referenser: 18 Dokumenttyp: Översikt UI-nummer: 06101184

Tidskrift

Ugeskrift for Laeger 2006;168(43)3704-9 ISSN 0041-5782 E-ISSN 1603-6824 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

Fragile X syndrome (FXS) is the most prevalent cause of inherited mental retardation, and calculations show that there are approximately 700 non-diagnosed cases in Denmark. Since the disease is severe, screening for FXS should be considered in order to improve genetic counselling. International experience indicates that efforts should initially be on active case finding among persons with learning difficulties and subsequently on cascade screening to identify carriers. Prenatal screening programmes may be an option when reliable high-throughput diagnostic methods are available.