Pregled bibliografske jedinice broj: 388243
Genetic thrombophilia and pregnancy complications
Genetic thrombophilia and pregnancy complications, 2008. (ostalo).
CROSBI ID: 388243 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetic thrombophilia and pregnancy complications
Autori
Lenz, Bahrija ; Kvolik, Slavica ; Grahovac, Blaženka.
Izvornik
Clinical Chemistry and Laboratory Medicine
Vrsta, podvrsta
Ostale vrste radova, ostalo
Godina
2008
Ključne riječi
Pregnancy complications; Factor V Leiden; prothrombin 20210G; MTHFR 677C
Sažetak
At least one thrombophilic mutation was observed in 41.6% of women with pregnancy complications vs. to 20.6% of women with normal pregnancies (p=0.003), factor V Leiden was observed in 15.8% cases and 7.8% controls, prothrombin 20210A in 5.9% cases and 2.9% controls and homozygosity for MTHFR 677T, in 19.8% cases and 9.8% controls. Double and triple thrombophilic mutations were detected in 6.9% women with pregnancy complications compared to none in the control group. Women with severe pregnancy complications and related venous thromboembolism have an increased frequency of genetic thrombophilic mutations.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
Napomena
Rad je prikazan kao kongresno priopćenje na 7th International Symposium on Molecular Diagnostics, Medical University of Graz, Austria, May 22 – 24 2008 (A65)i štampan u Clin Chem Lab Med 2008 ; 46(4):45– A66 (Walter de Gruyter • Berlin • New York. DOI 10.1515/CCLM.2008.05)
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Osijek,
Medicinski fakultet, Osijek