{"id":2453,"date":"2022-10-24T12:50:11","date_gmt":"2022-10-24T11:50:11","guid":{"rendered":"https:\/\/trisomytest1.wpengine.com\/?page_id=2453"},"modified":"2024-07-02T11:55:01","modified_gmt":"2024-07-02T10:55:01","slug":"what-is-babygen","status":"publish","type":"page","link":"https:\/\/babygen.sk\/en\/what-is-babygen\/","title":{"rendered":"What is BabyGen"},"content":{"rendered":"

BabyGen <\/strong>is a molecular test
\nto determine the sex of the foetus<\/p>\n<\/div><\/div>

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Unique<\/b><\/p>\n<\/div><\/div>

It can analyse the widest range of fetal chromosomal disorders across the entire genome from as early as 11. week of pregnancy.<\/p>\n<\/div><\/div><\/div><\/div>

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Reliable<\/b><\/p>\n<\/div><\/div>

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More than 99.5% accuracy<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Comprehensive<\/strong><\/p>\n<\/div><\/div>

It provides detailed fetal DNA screening and free verification of a positive result by amniotic fluid testing with the GenomeScreen prenatal test.<\/p>\n<\/div><\/div><\/div><\/div><\/div>

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Painless<\/strong><\/p>\n<\/div><\/div>

Examination of the mother’s blood.<\/p>\n<\/div><\/div><\/div><\/div>

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Quick<\/strong><\/p>\n<\/div><\/div>

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Result available from week 10.<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Secure<\/strong><\/p>\n<\/div><\/div>

No risk to the fetus.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

Answers hidden in the blood<\/h3>\n<\/div><\/div>

BabyGen is a non-invasive genetic screening test for fetal sex<\/b>, which is performed in a genetic laboratory by analysing a sample of the mother’s blood, from as early as 10. week of pregnancy. Sensitive molecular methods based on DNA analysis can identify the presence of the Y chromosome in the blood of a pregnant woman. It is currently the most accurate prenatal test of fetal sex, determining the result with more than 99.5% accuracy<\/b>.*<\/sup><\/p>\n

*<\/sup> The result is validated on more than 1500 retrospectively and prospectively analysed samples of pregnant women.<\/em><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

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Sex vs. hereditary disease<\/h3>\n<\/div><\/div>

Sex vs. hereditary disease<\/h3>\n<\/div><\/div>

Knowing the sex of your baby before birth is not only something future parents want to do out of curiosity, but also if the sex of the baby matters from a health point of view. This may be due, for example, to the presence of a hereditary disease that is sex-linked<\/b>. The most common examples are haemophilia and Duchenne muscular dystrophy, which is the most severe form of muscular dystrophy ever.<\/p>\n

Thus, in the case of clinically indicated sex determination, the mother-to-be does not necessarily have to undergo an invasive procedure in which the doctor takes amniotic fluid samples directly from the uterus.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

TRISOMY Test<\/b><\/p>\n<\/div><\/div>

\"certifik\u00e1ty\"<\/div><\/div>

The sex of the fetus is also detected by the prenatal TRISOMY test<\/b>, which can also reliably rule out common fetal chromosomal disorders such as Down syndrome.
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\nMore about the TRISOMY test<\/a>
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