{"id":12658,"date":"2022-01-25T15:52:29","date_gmt":"2022-01-25T14:52:29","guid":{"rendered":"https:\/\/www.laboratoriogenoma.eu\/analisi_en\/prenatalsafe-3-_en\/"},"modified":"2026-04-22T10:26:13","modified_gmt":"2026-04-22T08:26:13","slug":"prenatalsafe-3-_en","status":"publish","type":"post","link":"https:\/\/www.laboratoriogenoma.eu\/en\/analisi_en\/prenatalsafe-3-_en\/","title":{"rendered":"PrenatalSafe\u00ae 3"},"content":{"rendered":"<p>PrenatalSafe&reg; is a non-invasive prenatal test (NIPT) based on cell-free fetal DNA analysis from maternal plasma that screens for chromosomal abnormalities in the fetus.<br \/>\nPrenatalSafe&reg;3 is a screening test for Trisomy 21, Trisomy 18, Trisomy 13 and fetal sex (optional).<br \/>\nPrenatalSafe&reg; 3 is suitable for both singleton o twin pregnancies.<br \/>\nPrenatalSafe&reg; 3 can be integrated, for free, with RhSafe&reg; test, a non-invasive prenatal exam that, analyzing the fetal DNA isolated from a blood sample of the mother to be, allows to determine fetal Rh(D) Factor. RhSafe&reg; test is optional, and is performed for free (on request) in Rh(D) negative pregnant women, with a Rh(D) positive male partner.<br \/>\n&nbsp;<br \/>\n&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>PrenatalSafe&reg; is a non-invasive prenatal test (NIPT) based on cell-free fetal DNA analysis from maternal plasma that screens for chromosomal abnormalities in the fetus. PrenatalSafe&reg;3 is a screening test for Trisomy 21, Trisomy 18, Trisomy 13 and fetal sex (optional). PrenatalSafe&reg; 3 is suitable for both singleton o twin pregnancies. PrenatalSafe&reg; 3 can be integrated, [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[33520,36529,36096,36095,36094,33570,33603,33569,33548],"tags":[],"class_list":["post-12658","post","type-post","status-publish","format-standard","hentry","category-analisi_en","category-cfdna_en","category-chr13_en","category-chr18_en","category-chr21_en","category-gynecology_en","category-ngs_en","category-prenatal-diagnosis_en","category-prenatalsafe_en"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/posts\/12658","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/comments?post=12658"}],"version-history":[{"count":1,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/posts\/12658\/revisions"}],"predecessor-version":[{"id":14823,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/posts\/12658\/revisions\/14823"}],"wp:attachment":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/media?parent=12658"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/categories?post=12658"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/tags?post=12658"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}