Factor XI deficiency in women

被引:0
作者
Kadir, RA
Economides, DL
Lee, CA
机构
[1] Royal Free Hosp, Hemophilia Ctr, London NW3 2QG, England
[2] Royal Free Hosp, Hemostasis Unit, London NW3 2QG, England
[3] Royal Free Hosp, Univ Dept Obstet & Gynecol, London NW3 2QG, England
关键词
factor XI; pregnancy; menstruation;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Factor XI (FXI) deficiency is an uncommon autosomally transmitted coagulopathy found predominantly in Jewish kindreds. It is associated with variable bleeding tendency that usually manifests after trauma, surgery, or other challenges to hemostasis. Therefore, women with FXI deficiency are at risk of excessive bleeding during their menstrual periods, childbirth, and after surgery. Increased awareness and close collaboration among hematologists, obstetricians, and gynecologists and availability of management guidelines is essential to minimize these risks. This review provides data from current research in FXI deficiency and pregnancy care, menstrual problems, and the role of screening for this disorder in women referred with menorrhagia. (C) 1999 Wiley-Liss, Inc.
引用
收藏
页码:48 / 54
页数:7
相关论文
共 62 条
  • [1] FACTOR-XI AND FACTOR-XII AND PREKALLIKREIN IN SICK AND HEALTHY PREMATURE-INFANTS
    ANDREW, M
    BHOGAL, M
    KARPATKIN, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (19) : 1130 - 1133
  • [2] DEVELOPMENT OF THE HUMAN COAGULATION SYSTEM IN THE FULL-TERM INFANT
    ANDREW, M
    PAES, B
    MILNER, R
    JOHNSTON, M
    MITCHELL, L
    TOLLEFSEN, DM
    POWERS, P
    [J]. BLOOD, 1987, 70 (01) : 165 - 172
  • [3] FACTOR-XI (PLASMA THROMBOPLASTIN ANTECEDENT) DEFICIENCY IN ASHKENAZI JEWS IS A BLEEDING DISORDER THAT CAN RESULT FROM 3 TYPES OF POINT MUTATIONS - (COAGULATION GENETIC-DEFECT POLYMERASE CHAIN-REACTION)
    ASAKAI, R
    CHUNG, DW
    RATNOFF, OD
    DAVIE, EW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) : 7667 - 7671
  • [4] FACTOR-XI DEFICIENCY IN ASHKENAZI JEWS IN ISRAEL
    ASAKAI, R
    CHUNG, DW
    DAVIE, EW
    SELIGSOHN, U
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (03) : 153 - 158
  • [5] BOLTONMAGGS PHB, 1995, THROMB HAEMOSTASIS, V73, P194
  • [6] INHERITANCE AND BLEEDING IN FACTOR-XI DEFICIENCY
    BOLTONMAGGS, PHB
    WANYIN, BY
    MCCRAW, AH
    SLACK, J
    KERNOFF, PBA
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1988, 69 (04) : 521 - 528
  • [7] THROMBOGENIC POTENTIAL OF FACTOR-XI CONCENTRATE
    BOLTONMAGGS, PHB
    COLVIN, BT
    SATCHI, G
    LEE, CA
    LUCAS, GS
    [J]. LANCET, 1994, 344 (8924) : 748 - 749
  • [8] BOLTONMAGGS PHB, 1992, THROMB HAEMOSTASIS, V67, P314
  • [9] Bonnar J, 1980, J Clin Pathol Suppl (R Coll Pathol), V14, P55, DOI 10.1136/jcp.33.Suppl_14.55
  • [10] BONNAR J, 1996, BRIT MED J, V313, P578