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Quebec platelet disorder

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Description

Quebec platelet disorder is an autosomal dominant bleeding disorder due to a gain-of-function defect in fibrinolysis. Although affected individuals do not exhibit systemic fibrinolysis, they show delayed onset bleeding after challenge, such as surgery. The hallmark of the disorder is markedly increased PLAU levels within platelets, which causes intraplatelet plasmin generation and secondary degradation of alpha-granule proteins. The disorder shows a favorable therapeutic response to fibrinolytic inhibitors (summary by Diamandis et al., 2009).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

62

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Genes

External Links

  • OMIM

    601709

  • Orphanet

    220436

  • HPO
  • Medgen

    C1866423

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