{"id":2564,"date":"2022-12-28T09:06:48","date_gmt":"2022-12-28T08:06:48","guid":{"rendered":"https:\/\/trisomytest1.wpengine.com\/?page_id=2564"},"modified":"2023-09-04T13:35:10","modified_gmt":"2023-09-04T12:35:10","slug":"trisomy-test-complete-cystic-fibrosis","status":"publish","type":"page","link":"https:\/\/trisomytest.sk\/en\/trisomy-test-complete-cystic-fibrosis\/","title":{"rendered":"TRISOMY test Complete +Cystic fibrosis"},"content":{"rendered":"

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

+Cystic fibrosis<\/p>\n<\/div><\/div>

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

TRISOMY<\/strong> test Complete\u00a0<\/strong>+ Cystic Fibrosis<\/strong> is an additional assessment that\u00a0can be ordered together with TRISOMY test Complete<\/a><\/span>. The test covers an assessment detecting the most common F508del mutation in the CFTRgene causing Cystic Fibrosis, which is one of the most common severe hereditary diseases. 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>

590 \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>

In addition to the most common trisomies of chromosomes 21, 18, 13, the test also reveals the so-called rare changes in the number of any of the chromosomes, including sex chromosomes, which may be associated with possible complications during pregnancy.<\/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 while minimizing the need for amniocentesis (invasive collection of a sample of amniotic fluid).<\/p>\n<\/div><\/div><\/div><\/div>

The presence of the F508del mutation in the CFTR gene which represents the most common mutation causing cystic fibrosis in the Caucasoid population.<\/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> + CYSTIC FIBROSIS may be taken by a pregnant woman at her own request and after a consultation with a specialists in medical genetics. The test is suitable for any pregnant woman starting from the 11th week of pregnancy if:<\/p>\n<\/div><\/div>