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Inherited Thrombophilia

  • Radboud University Nijmegen

Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review

Abstract

Thrombophilia can be defined as laboratory abnormalities, usually in the coagulation system, that result in a hypercoagulable state and thus predispose to thrombosis. These abnormalities may be acquired or inherited. The most clearly established form of acquired thrombophilia is the antiphospholipid anti- body syndrome. This chapter focuses on inherited thrombophilia. The relevance of inherited thrombophilia in early pregnancy is manifested in an elevated risk of venous thromboembolism, a modestly increased risk of miscarriage, and a possible relation with fertility.
Original languageEnglish
Title of host publicationEarly Pregnancy, Third Edition
PublisherCambridge University Press
Pages122-136
Number of pages15
ISBN (Electronic)9781009532549
ISBN (Print)9781009532501
DOIs
Publication statusPublished - 1 Jan 2025
Externally publishedYes

Publication series

NameEarly Pregnancy, Third Edition

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acetylsalicylic acid
  • Anticoagulants
  • Antithrombin deficiency
  • Factor V Leiden
  • Low-molecular-weight heparin
  • Protein C deficiency
  • Protein S deficiency
  • Prothrombin G20210A mutation
  • Thrombophilia
  • Venous thromboembolism

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