{"id":33545,"count":2,"description":"<strong>GeneSafe<strong>&reg;<\/strong><\/strong>&nbsp;is the first non-invasive prenatal test that screens for both&nbsp;de novo&nbsp;and&nbsp;inherited single-gene disorders.&nbsp;Current non-invasive prenatal tests screen for aneuploidies and microdeletions.&nbsp;<strong>PrenatalSafe&reg;&nbsp;Karyo<\/strong>&nbsp;also screens for rare aneuploidies and segmental chromosome imbalances (gains and losses) in every chromosome in the fetal genome, providing karyotype-level insight.\r\n<strong>GeneSafe<strong>&reg;<\/strong>&nbsp;<\/strong>goes further.\r\nThrough&nbsp;cfDNA&nbsp;analysis from maternal plasma, it&nbsp;screens for several clinically significant and life-altering genetic disorders that are not screened for with current NIPT technology.\r\n<strong>GeneSafe<strong>&reg;<\/strong><\/strong>&nbsp;involves 3 different levels of screening:&nbsp;Inherited,&nbsp;<em>de novo<\/em>&nbsp;and Complete.","link":"https:\/\/www.laboratoriogenoma.eu\/en\/category\/analisi-madre_en\/genesafe_en\/","name":"GeneSafe\u00ae","slug":"genesafe_en","taxonomy":"category","parent":33519,"meta":[],"acf":[],"_links":{"self":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/categories\/33545","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/categories"}],"about":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/taxonomies\/category"}],"up":[{"embeddable":true,"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/categories\/33519"}],"wp:post_type":[{"href":"https:\/\/www.laboratoriogenoma.eu\/en\/wp-json\/wp\/v2\/posts?categories=33545"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}