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Combined inherited thrombophilia is the simultaneous occurrence of hereditary gene defects in coagulation factors, anticoagulant proteins, enzymes involved in coagulation, or other inherited factors. Patients with these combined genetic mutations have a high risk of thrombosis, and they can also be prone to an increased risk of recurrent abortions. In this setting, various methods, including functional assays, molecular studies, and immunological assays, may be used for the detection of underlying causes of combined thrombophilia.

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Laboratory Diagnosis of Combined Inherited/Genetic Thrombophilia

  • 章节

  • 发表日期：

    2025年

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  • Alieh Fazeli,
  • Mahmood Shams,
  • Ali Dabbagh,
  • Magy Abdelwahab

摘要

Combined inherited thrombophilia is the simultaneous occurrence of hereditary gene defects in coagulation factors, anticoagulant proteins, enzymes involved in coagulation, or other inherited factors. Patients with these combined genetic mutations have a high risk of thrombosis, and they can also be prone to an increased risk of recurrent abortions. In this setting, various methods, including functional assays, molecular studies, and immunological assays, may be used for the detection of underlying causes of combined thrombophilia.