Von Willebrand disease and other bleeding disorders in women: consensus on diagnosis and management from an international expert panel.

نویسندگان

  • Andra H James
  • Peter A Kouides
  • Rezan Abdul-Kadir
  • Mans Edlund
  • Augusto B Federici
  • Susan Halimeh
  • Pieter W Kamphuisen
  • Barbara A Konkle
  • Oscar Martínez-Perez
  • Claire McLintock
  • Flora Peyvandi
  • Rochelle Winikoff
چکیده

Reproductive tract bleeding in women is a naturally occurring event during menstruation and childbirth. In women with menorrhagia, however, congenital bleeding disorders historically have been underdiagnosed. This consensus is intended to allow physicians to better recognize bleeding disorders as a cause of menorrhagia and consequently offer effective disease-specific therapies.

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منابع مشابه

von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA).

von Willebrand disease (VWD) is a commonly encountered inherited bleeding disorder affecting both males and females, causing mucous membrane and skin bleeding symptoms, and bleeding with surgical or other haemostatic challenges. VWD may be disproportionately symptomatic in women of child-bearing age. It may also occur less frequently as an acquired disorder (acquired von Willebrand syndrome). V...

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Evaluation of Normal Range of Bleeding Scores in Healthy Iranian Adults using the International Society on Thrombosis and Hemostasis Bleeding Assessment Tool

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The role of exon 45 and 16 in the pathogenesis of Von Willebrand disease in Iranian Patients

Abstract Background Von Willebrand disease (VWD) is an autosomal recessive congenital bleeding disorder with deficiency or dysfunction of von Willebrand factor (VWF). The gene encoding for the VWF is located on chromosome 12, which is 178 Kb with 52 exons. Various mutations of this gene is responsible for the clinical features of VWD, but some single nucleotide polymorphisms make the molecu...

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Frequency Assessment of the H817Q (2451T→A) Variant of von Willebrand Gene in Individuals without Hemorrhagic Signs

Abstract Background and Aims:‎ Von Willebrand disease is a bleeding disorder caused by quantitative or functional defects in von Willebrand factor. The disease is found in up to 1 percent of the population. The most common symptom is mucocutaneous bleeding. Recently, studies conducted on healthy people showed that the H817Q mutation that previously known to cause von Willebrand...

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SOGC CLINICAL PRACTICE GUIDELINES Gynaecological and Obstetric Management of Women With Inherited Bleeding Disorders

Objective: The prevalence of bleeding disorders, notably von Willebrand disease (vWD), among adult women with objectively documented menorrhagia is consistently reported to be 10% to 20% and is even higher in adolescents presenting with menorrhagia. This consensus document has been developed by a multidisciplinary committee consisting of an anesthesiologist, 2 hematologists, and an obstetrician...

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عنوان ژورنال:
  • American journal of obstetrics and gynecology

دوره 201 1  شماره 

صفحات  -

تاریخ انتشار 2009