TRISOMY test is suitable for any pregnant woman from the 12th week of pregnancy onward.

Every pregnant woman can undergo the trisomy test at her own request if she wants to be sure her unborn baby does not develop trisomy 21, 18 or 13 monitored by the test. Chromosomal abnormalities cause up to 85 % of serious genetic fetal disorders.

TRISOMY test is particularly suitable for pregnant women:

  • who have increased concerns about any potential disability of their baby caused by one of the trisomy types the test is designed to monitor,
  • who give birth over the age of 35 and whose biochemical screening test results are negative (integrated test, double test, triple test or combined test),
  • who conceived as a result of IVF,
  • with positive biochemical screening which must be confirmed by further examination (amniocentesis),*
  • whose ultrasound screening test results suggest a higher risk of trisomy 21, 18 or 13,*
  • who have already been diagnosed with a chromosomal abnormality of their fetus before,*
  • who have suffered recurrent miscarriage*
  • who want to avoid amniocentesis, or suffer complications which can increase its risk, such as: higher risks of miscarriage, low levels of blood clotting, immunization risks due to Rh incompatibility (Rh-negative), being in the period between the 14th and the 16th week of pregnancy, uterine fibroids and placenta praevia.

* The test must be preceded by a genetic consultation.

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