{"id":12609,"date":"2026-02-13T18:48:38","date_gmt":"2026-02-13T15:48:38","guid":{"rendered":"https:\/\/nesiller.com\/single-gene-tests\/"},"modified":"2026-10-03T18:35:14","modified_gmt":"2026-10-03T15:35:14","slug":"single-gene-tests","status":"publish","type":"page","link":"https:\/\/nesiller.com\/en\/prenatal-testing\/single-gene-tests\/","title":{"rendered":"Single Gene Tests"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"12609\" class=\"elementor elementor-12609 elementor-11998\" data-elementor-post-type=\"page\">\n\t\t\t\t<div data-ekitparallax=\"{&quot;ekit_section_parallax_bg&quot;:&quot;yes&quot;,&quot;ekit_section_parallax_bg_speed&quot;:0.5,&quot;elementor_lazy_load&quot;:&quot;1&quot;}\" class=\"elementor-element elementor-element-26d766b e-flex e-con-boxed e-con e-parent\" data-id=\"26d766b\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-5663116 e-con-full e-flex e-con e-child\" data-id=\"5663116\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-8ad181b section-title at-heading-animation at-animation-heading-none elementor-invisible elementor-widget elementor-widget-heading\" data-id=\"8ad181b\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeInUp&quot;,&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<div class=\"elementor-heading-title elementor-size-default\"><a href=\"https:\/\/nesiller.com\/en\/prenatal-testing\/\">Prenatal Tests<\/a><\/div>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-0d49767 elementor-widget elementor-widget-heading\" data-id=\"0d49767\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">Single Gene Testing<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-66c7184 elementor-invisible elementor-widget elementor-widget-text-editor\" data-id=\"66c7184\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeInUp&quot;,&quot;_animation_delay&quot;:200,&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>From Uncertainty to Clarity in Prenatal Diagnosis<\/p>\t\t\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<div class=\"elementor-element elementor-element-e856ea1 e-flex e-con-boxed e-con e-parent\" data-id=\"e856ea1\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-ce6fc12 elementor-widget elementor-widget-text-editor\" data-id=\"ce6fc12\" data-element_type=\"widget\" data-e-type=\"widget\" data-settings=\"{&quot;ekit_we_effect_on&quot;:&quot;none&quot;}\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>Disease-causing (pathogenic) genetic variants previously identified in family members can be directly analyzed, providing accurate and timely guidance for families with a history of genetic disorders.<\/p><p>Pathogenic variants identified through parental carrier screening can, where technically feasible and clinically appropriate, be evaluated using prenatal single-gene testing to determine the genetic status of the fetus. (See:<a href=\"https:\/\/nesiller.com\/en\/carrier-screening\/\"><span style=\"text-decoration: underline;\"> <strong>IntelliGene Carrier Screening<\/strong><\/span><\/a>)<\/p><p>To help clarify clinically suspected structural anomalies or findings associated with a family history during pregnancy, we offer comprehensive prenatal panels targeting the most common single-gene disorders, including:<\/p><ul><li>Noonan Syndrome and RASopathies Panel,<\/li><li>CAKUT (Congenital Anomalies of the Kidney and Urinary Tract) Panel,<\/li><li>Tuberous Sclerosis and Neurocutaneous Syndromes Panel,<\/li><li>Skeletal Dysplasias and Osteogenesis Imperfecta Panel,<\/li><li>Holoprosencephaly (HPE) Panel and additional panels for other single-gene disorders.<\/li><\/ul>\t\t\t\t\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":"<p>Prenatal Tests Single Gene Testing From Uncertainty to Clarity in Prenatal Diagnosis [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":12699,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"footnotes":""},"class_list":["post-12609","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12609","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/comments?post=12609"}],"version-history":[{"count":21,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12609\/revisions"}],"predecessor-version":[{"id":20829,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12609\/revisions\/20829"}],"up":[{"embeddable":true,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12699"}],"wp:attachment":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/media?parent=12609"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}