TromboNIM®


Genetic test for hereditary thrombophilia.

Home » Services » TromboNIM: Hereditary thrombophilia test

Genetic test for hereditary thrombophilia designed to identify patients with an increased risk of developing thromboembolic disease. NIMGenetics offers a comprehensive updated test with a risk estimation based on specific quantitative criteria for each of the genomic positions analysed.

It analyses 24 variants in 18 genes associated with increased thrombotic risk. Includes genes involved in multiple molecular pathways implicated in hereditary thrombophilia.

¿WHEN IS IT INDICATED?

Genetic thrombophilia tests are indicated in the following situations:

  • Personal history of thromboembolic disease:
    • Deep vein thrombosis or recurrent thrombophlebitis
    • Pulmonary embolism
    • Recurrent miscarriages
  • Treatment with oral contraceptives, hormone replacement therapy and fertilisation cycles.
  • Family history of venous thrombosis.
  • Other risk conditions: pregnancy, obesity, smoking, older age, conditions associated with thrombophilia and prolonged immobilisation.

 

Turnaround time: 15 working days from receipt of the sample.
Reference:  PEG7001

Please remember to attach the Application Form and Informed Consent Form to the sample, which you will find on the right.

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