Book Inherited Thrombophilia Panel | Lahalak Medical Platform

This panel identifies genetic causes of recurrent pregnancy loss and placental issues, helping you plan a safer pregnancy with specialized medical supervision to ensure the well-being of both mother and baby.

Scientific name: Inherited Thrombophilia Panel for Pregnancy Complications

Advanced genetic testing covering Factor V Leiden, Prothrombin mutations, and Protein C/S deficiency to assess blood clotting risks that may lead to pregnancy complications or recurrent loss.

Inherited Thrombophilia Panel for Pregnancy Complications - Ensure a Safe Future Pregnancy
Service type Laboratory test
Duration 10-15 minutes
Fasting Fasting is not required

Included Services

  • Factor V Leiden Mutation Test
  • Prothrombin Gene Mutation Test
  • Protein C Activity Level
  • Protein S Activity Level

Medical Service Information

Purpose of the Panel

  • Identify underlying genetic causes of recurrent miscarriage.
  • Assess the risk of developing deep vein thrombosis (DVT) during pregnancy.
  • Develop a preventive plan involving anticoagulants if necessary.

Target Groups

  • Women who have experienced two or more pregnancy losses.
  • Cases of premature placental abruption in previous pregnancies.
  • Individuals with a strong family history of blood clots.

Results and Follow-up

  • Results are typically available within 7 to 10 working days.
  • Results should be discussed with a feto-maternal specialist or hematologist.
  • A positive result requires medical prophylaxis rather than immediate alarm.

Conditions & Notices

  • Preferably performed when not on anticoagulants
  • Inform the doctor about family medical history

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