The spectrum of bleeding disorders in women with menorrhagia: A report from Western India

Sucheta A. Trasi, Anil V. Pathare, Shrimati D. Shetty, Kanjaksha Ghosh*, Vinita Salvi, Dipika Mohanty

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

28 Citations (Scopus)


In order to evaluate the incidence of hereditary bleeding disorders in patients presenting with menorrhagia, where the usual gynecological and endocrinal causes of bleeding were ruled out by various local ultrasonography (USG) and relevant endocrine investigations, 120 women aged between 18 and 35 years presenting with menorrhagia without any discernable cause were studied using an open design, where the investigators knew that these patients had menorrhagia. These patients were investigated for inherited coagulation defects. Of the 120 women investigated, 19.16% (23 cases) had an inherited coagulation disorder to account for their menorrhagia. Although a majority (11.6%) are patients with von Willebrand's disease (VWD), other rare platelet disorders such as Glanzmann's thrombasthenia (3.3%), Bernard-Soulier syndrome (0.83%), coagulation factor deficiencies such as factor VIII (0.83%), factor X (0.83%), and factor XI (0.83%), and immune thrombocytopenia (0.83%) were also found. Taking a detailed history for bleeding from other sites howsoever minor, paternal consanguinity as well as family history of bleeding tendencies appeared as a very strong predictor for such kinds of disease in patients with menorrhagia. Patients with menorrhagia without a discernable cause, therefore, need evaluation for the congenital coagulation disorders.

Original languageEnglish
Pages (from-to)339-342
Number of pages4
JournalAnnals of Hematology
Issue number5
Publication statusPublished - May 2005
Externally publishedYes


  • Bleeding disorders
  • India
  • Menorrhagia
  • Von Willebrand's disease

ASJC Scopus subject areas

  • Hematology


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