Results of multicenter registry for patients with inherited factor VII deficiency in Turkey.
Aydan AkdenizAyşegül ÜnüvarMuhlis Cem ArEsra PekpakArzu AkyayÖzgür MehtaFatma Keklik KaradağCan AcipayamAli DoğanÖmer EkinciSultan Aydın KökerCanan AlbayrakUfuk DemirciTekin GüneyMeltem KurtSerap KaramanÖzge Şahin KimyonSinan AlbayrakYurday ÖncülSerkan ÜnalFahri ŞahinRumeysa TunaBulent ZulfikarBurcu Belen ApakElif Gülsüm ÜmitAhmet Muzaffer DemirPublished in: Scandinavian journal of clinical and laboratory investigation (2021)
Our data are consistent with most of the published literature in terms of cut-off FVIIL for bleeding, as well as reasons for prophylaxis, showing both an increased severity of bleeding and younger age at diagnosis with decreasing FVIIL. However, in order to offer a classification similar to that in Hemophilia A or B, data of a larger cohort with information about environmental and genetic factors are required.
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