Abstract
The congenital Factor VII deficiency (FVIID) is a rare hemorrhagic disorderwith an autosomal recessive pattern of inheritance and a prevalence of 1:500,000. In 1994 the International Greifswald Registry of congenital FVII deficiency was initiated [1]. We analyzed the phenotype and genotype of subjects,who presented with reduced FVII activities.
order of the physicians according to the number of registered admissions/CRFs.
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Herrmann FH, Wulff K, Auberger K, Aumann V, Bergmann F, Bergmann K, Bratanoff E, Franke D, Grundeis M, Kreuz W, Lenk H, Losonczy H, Maak B, Marx G, Mauz-Körholz Ch, Pollmann H, Serban M, Sutor A, Syrbe G, Vogel G, Weinstock N, Wenzel E and Wolf K. Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency. Semin. Thromb.Hemost. 2000; 26: 293–400
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Ingerslev K, Christiansen K and Soerensen B for the International Registry on Factor VII Deficiency (IRF7) Steering Committee. Inhibitor to factor VII deficiency: detection and course of the inhibitory response. J Thromb Haemost 2005; 799–800
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Herrmann, F.H. et al. (2008). Therapeutical Options for Congenital FVII Deficiency — The HK 7 Project of the International Greifswald Registry of the Congenital FVII Deficiency (GR-HK-7). In: Scharrer, I., Schramm, W. (eds) 37th Hemophilia Symposium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-73535-9_52
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DOI: https://doi.org/10.1007/978-3-540-73535-9_52
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