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MTHFR C 677T mutation and 4G/5G PAI-1 polymorphism in patient with polycystic ovarian syndrome (CROSBI ID 140740)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Radaković, Branko ; Šprem, Marina MTHFR C 677T mutation and 4G/5G PAI-1 polymorphism in patient with polycystic ovarian syndrome // Collegium antropologicum, 31 (2007), 3; 919-921

Podaci o odgovornosti

Radaković, Branko ; Šprem, Marina

engleski

MTHFR C 677T mutation and 4G/5G PAI-1 polymorphism in patient with polycystic ovarian syndrome

Combined oral contraceptives (Ocs) are the most commonly used androgen suppressors and the treatment of choice for menstrual dysfunction in women with polycystic ovarian syndrome (PCOs). Although OCs have remained popular due to their convenience and effectiveness, there have been continuing concerns about adverse effects. The OCs have long been known to incur and increased risk of venous thromboembolism especially in carriers of common inherited thromboembolic defects. Factor V Leiden, prothrombin factor G20210A polymorphism, MTHFR (C677T) mutation and 4G/5G polymorphism of the PAI-1 gene account for the majority of thromboembolic events in association with oral contraceptive use. The aim of the article is to present woman with unrecognized inherited thrombophilia who was treated with OCs due to PCOs signs.

PCOS; oral contraceptives; factor V Leiden; prothrombin factor G20210A polymorphism; MTHFR (C677T) mutation; 4G/5G polymorphism PAI-1 gene

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Podaci o izdanju

31 (3)

2007.

919-921

objavljeno

0350-6134

Povezanost rada

Kliničke medicinske znanosti

Indeksiranost