{"id":15717,"date":"2026-07-02T12:48:36","date_gmt":"2026-07-02T09:48:36","guid":{"rendered":"https:\/\/bak.lt\/paslaugos\/nipt-non-invasive-prenatal-testing\/"},"modified":"2026-07-02T12:48:38","modified_gmt":"2026-07-02T09:48:38","slug":"nipt-non-invasive-prenatal-testing","status":"publish","type":"paslaugos","link":"https:\/\/bak.lt\/en\/services\/nipt-non-invasive-prenatal-testing\/","title":{"rendered":"NIPT \u2013 non-invasive prenatal testing"},"content":{"rendered":"\t\t
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NIPT \u2013 peace of mind for your baby’s health.<\/strong><\/p>\r\n\r\n

Pregnancy should be a time of joy, not anxiety. Screening tests performed during pregnancy are known as non-invasive prenatal testing (NIPT) \u2013 the safest way, from as early as the 10th week of pregnancy for a singleton pregnancy, and from the 12th week of pregnancy for a twin pregnancy,<\/strong> to ensure the foetus is developing normally.<\/p>\r\n\r\n

Why choose NIPT?<\/p>\r\n\r\n

\u2022 Unmatched accuracy<\/strong>: The NIPT test analyses foetal DNA, meaning its accuracy in detecting the most common abnormalities is over 99%. The test assesses the risk of the following syndromes: Down’s syndrome, Edwards’ syndrome, and Patau’s syndrome.<\/p>\r\n\r\n

If you want maximum reassurance, we recommend a comprehensive (whole-genome) NIPT. It screens not only the primary chromosomes but also minor structural changes in them that could affect child development (such as Turner’s, Klinefelter’s, DiGeorge, and other syndromes).<\/p>\r\n\r\n

\u2022 Complete safety<\/strong>: This is simply a routine blood sample taken from your vein. The procedure is 100% safe, carrying no risk to the pregnancy.<\/p>\r\n\r\n

\u2022 Fast results<\/strong>: You will receive your accurate results, including the baby’s sex (if requested), in just 5 to 10 working days.<\/p>\r\n\r\n

Give yourself the opportunity to wait with peace of mind.<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Placenta Safe\u2122 Rh \u2013 foetal RhD status determination<\/strong><\/p>\r\n

Placenta Safe\u2122 Rh \u2013 a specialised non-invasive prenatal test that allows for the safe and reliable determination of the foetal RhD status. This test is intended for pregnant women with an RhD-negative blood group, if the baby’s father’s blood group is RhD-positive.<\/em><\/p>\r\n\r\n

myPrenatal 3T \u2013 Minimal NIPT for analysis of chromosomes 21, 18, and 13<\/strong><\/p>\r\n

Detects the three most common foetal chromosomal trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome).<\/p>\r\n\r\n

myPrenatal BASIC \u2013 Minimal NIPT for analysis of chromosomes 21, 18, and 13<\/strong><\/p>\r\n

Detects the three most common foetal chromosomal trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex.<\/p>\r\n\r\n

Placenta Safe\u2122 3 \u2013 Minimal NIPT for analysis of chromosomes 21, 18, and 13<\/strong><\/p>\r\n

Detects the three most common foetal chromosomal trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex.<\/p>\r\n

In the case of twin pregnancies, the test determines whether at least one foetus has a trisomy, and whether at least one foetus is male. Sex chromosome abnormalities are not screened in twin pregnancies.<\/em><\/p>\r\n\r\n

myPrenatal\u00ae XY \u2013 Basic NIPT with sex chromosome analysis (performed only for singleton pregnancies)<\/strong><\/p>\r\n

Detects the three primary trisomies, foetal sex, and sex chromosome aneuploidies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), Trisomy 13 (Patau’s syndrome), foetal sex, and sex chromosome aneuploidies.<\/p>\r\n\r\n

Placenta Safe\u2122 5 \u2013 Basic NIPT with sex chromosome analysis<\/strong><\/p>\r\n

Detects the three primary trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex and sex chromosome aneuploidies.<\/p>\r\n

Suitable for singleton and twin monochorionic pregnancies. In the case of twin pregnancies, the test determines whether at least one foetus has a trisomy, and whether at least one is male. Sex chromosome abnormalities are not screened in twin pregnancies.<\/em><\/p>\r\n\r\n

myPrenatal\u00ae Genome \u2013 Expanded NIPT with sex chromosome, deletion, and duplication analysis<\/strong><\/p>\r\n

Detects the three primary trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex, sex chromosome aneuploidies, and large deletions and duplications (>7 Mb).<\/p>\r\n\r\n

Placenta Safe\u2122 Plus \u2013 Expanded NIPT with sex chromosome, deletion, and duplication analysis<\/strong><\/p>\r\n

Detects the three primary trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex, sex chromosome aneuploidies, microdeletions, microduplications, and trisomies 9 and 16.<\/p>\r\n

Suitable for singleton and twin monochorionic pregnancies. In the case of twin pregnancies, the test determines whether at least one foetus has a trisomy, and whether at least one is male. Sex chromosome abnormalities are not screened in twin pregnancies.<\/em><\/p>\r\n\r\n

myPrenatal Karyo \u2013 Comprehensive NIPT for all 23 chromosomes with deletion and duplication analysis<\/strong><\/p>\r\n

Detects the three primary trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex, sex chromosome aneuploidies, large deletions and duplications (>7 Mb), trisomies 9 and 16, and analysis of all chromosomes.<\/p>\r\n\r\n

Niptify \u2013 Comprehensive NIPT for all 23 chromosomes with deletion and duplication analysis<\/strong><\/p>\r\n

Detects the three primary trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex, sex chromosome aneuploidies, large deletions and duplications (>7 Mb), microdeletions, microduplications, trisomies 9 and 16, and analysis of all chromosomes.<\/p>\r\n

Performed only for singleton pregnancies.<\/em><\/p>\r\n\r\n

Placenta Safe\u2122 Karyo Plus \u2013 Comprehensive NIPT for all 23 chromosomes with deletion and duplication analysis<\/strong><\/p>\r\n

Detects the three primary trisomies: Trisomy 21 (Down’s syndrome), Trisomy 18 (Edwards’ syndrome), and Trisomy 13 (Patau’s syndrome), as well as foetal sex, sex chromosome aneuploidies, large deletions and duplications (>7 Mb), microdeletions, microduplications, trisomies 9 and 16, and analysis of all chromosomes.<\/p>\r\n

In the case of twin pregnancies, the test determines whether at least one foetus has a trisomy, and whether at least one is male. Sex chromosome abnormalities and microdeletions are not screened in twin pregnancies.<\/em><\/p>\r\n\r\n

Placenta Safe\u2122 Gene De Novo \u2013 NIPT for analysis of monogenic de novo and inherited conditions<\/strong><\/p>\r\n

Detects monogenic de novo conditions.<\/p>\r\n

Placenta Safe\u2122 Gene De Novo is a specialised NIPT designed to detect de novo (newly occurring) mutations that can cause syndromic or multi-system conditions. This test is particularly relevant if there is no family history of genetic disorders, but there is a risk of spontaneous genetic changes.<\/em><\/p>\r\n\r\n

Placenta Safe\u2122 Gene Complete \u2013 NIPT for analysis of monogenic de novo and inherited conditions<\/strong><\/p>\r\n

Detects monogenic de novo conditions and recessive inherited disorders.<\/p>\r\n

Placenta Safe\u2122 Gene Complete is the most comprehensive NIPT for monogenic disorders, covering both de novo mutations and several recessive conditions inherited from parents. This test provides valuable information on foetal genetic health.<\/em><\/p>\r\n\r\n

Placenta Safe\u2122 Complete Plus \u2013 ultimate NIPT for analysis of all 23 chromosomes, deletions, duplications, and genetic disorders<\/strong><\/p>\r\n

Detects the three primary trisomies, foetal sex, sex chromosome aneuploidies, large deletions and duplications (>7 Mb), microdeletions, microduplications, trisomies 9 and 16, analysis of all chromosomes, monogenic de novo conditions, recessive inherited disorders, and foetal Rhesus (RhD) status.<\/p>\r\n\r\n

Placenta Safe\u2122 Full Risk \u2013 ultimate NIPT for analysis of all 23 chromosomes, deletions, duplications, and genetic disorders<\/strong>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"

NIPT \u2013 peace of mind for your baby’s health. Pregnancy should be a time of joy, not anxiety. Screening tests performed during pregnancy are known as non-invasive prenatal testing (NIPT) \u2013 the safest way, from as early as the 10th week of pregnancy for a singleton pregnancy, and from the 12th week of pregnancy for […]<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"class_list":["post-15717","paslaugos","type-paslaugos","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/bak.lt\/en\/wp-json\/wp\/v2\/paslaugos\/15717"}],"collection":[{"href":"https:\/\/bak.lt\/en\/wp-json\/wp\/v2\/paslaugos"}],"about":[{"href":"https:\/\/bak.lt\/en\/wp-json\/wp\/v2\/types\/paslaugos"}],"version-history":[{"count":1,"href":"https:\/\/bak.lt\/en\/wp-json\/wp\/v2\/paslaugos\/15717\/revisions"}],"predecessor-version":[{"id":15718,"href":"https:\/\/bak.lt\/en\/wp-json\/wp\/v2\/paslaugos\/15717\/revisions\/15718"}],"wp:attachment":[{"href":"https:\/\/bak.lt\/en\/wp-json\/wp\/v2\/media?parent=15717"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}