{"id":2560,"date":"2022-11-03T10:00:15","date_gmt":"2022-11-03T09:00:15","guid":{"rendered":"https:\/\/trisomytest1.wpengine.com\/?page_id=2560"},"modified":"2025-12-09T10:56:35","modified_gmt":"2025-12-09T09:56:35","slug":"trisomy-test-complete","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/en\/trisomy-test-complete\/","title":{"rendered":"TRISOMY test Complete"},"content":{"rendered":"

TRISOMY test Complete<\/strong><\/p>\n<\/div><\/div>

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About the test<\/h3>\n<\/div><\/div>

TRISOMY<\/strong> test Complete<\/strong> is a comprehensive non-invasive prenatal screening test (NIPT) covering all 23 chromosome pairs which reliably reveals any chromosomal disorders across the entire fetal genome starting from the 11th week of pregnancy. The test delivers a detailed screening of fetal DNA while providing free verification of a positive result by testing of amniotic fluid using the GenomeScreen prenatal test. Before ordering the test, it is required that you read the latest version of the Information Concerning Genetic Laboratory Testing<\/a><\/span>.<\/p>\n<\/div><\/div><\/div><\/div>

The price of the test<\/p>\n<\/div><\/div>

530 \u20ac<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div>

chromosomal disorders<\/span><\/i><\/a><\/div>
hereditary diseases<\/span><\/i><\/a><\/div><\/div>

What does the test reveal?<\/p>\n<\/div><\/div>

Thanks to a detailed analysis of fetal DNA, the test will detect disorders in the number and amount of genetic material across all 23 pairs of chromosomes, both at the whole chromosomal and subchromosomal levels.<\/p>\n<\/div><\/div><\/div><\/div>

Thanks to a detailed analysis of fetal DNA, the test will detect disorders in the number and amount of genetic material across all 23 pairs of chromosomes, both at the whole chromosomal and subchromosomal levels.<\/p>\n<\/div><\/div><\/div><\/div>

The test can also detect deletions and duplications, which are mostly associated with clinically relevant fetal disorders. These cannot be detected by other commonly used prenatal screening methods.<\/p>\n<\/div><\/div><\/div><\/div><\/div>

It will also reveal any possible false positive results of biochemical prenatal screening.<\/p>\n<\/div><\/div><\/div><\/div>

It minimizes the need for amniocentesis (invasive collection of a sample of amniotic fluid).<\/p>\n<\/div><\/div><\/div><\/div>

If you are interested, the test can also determine the sex of the fetus.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

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TRISOMY<\/strong> test Complete<\/strong> may be taken by any pregnant woman at her own request after a consultation with a specialist in medical genetics. The test is suitable for any pregnant woman starting from the 11th week of pregnancy if:<\/p>\n<\/div><\/div>