{"id":12605,"date":"2026-02-13T18:51:33","date_gmt":"2026-02-13T15:51:33","guid":{"rendered":"https:\/\/nesiller.com\/cytogenetic-analysis\/"},"modified":"2026-10-03T18:35:10","modified_gmt":"2026-10-03T15:35:10","slug":"cytogenetic-analysis","status":"publish","type":"page","link":"https:\/\/nesiller.com\/en\/prenatal-testing\/cytogenetic-analysis\/","title":{"rendered":"Cytogenetic Analysis"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"12605\" class=\"elementor elementor-12605 elementor-12006\" 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\">Chromosomal Alterations<\/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>Chromosomal abnormalities account for <strong>50\u201360% of recurrent pregnancy losses<\/strong>. Numerical abnormalities (such as trisomies 13, 18, and 21) and structural chromosomal abnormalities are analyzed using FISH, chromosome analysis, and molecular karyotyping techniques.<\/p><p><b>Chromosome Analysis (Karyotyping)<\/b><\/p><table><tbody><tr><td><p><b>Feature<\/b><\/p><\/td><td><p><b>Details<\/b><\/p><\/td><\/tr><tr><td><p><b>Method<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">Cell Culture<\/span><\/p><\/td><\/tr><tr><td><p><b>Coverage<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">All chromosomes (24 chromosomes)<\/span><\/p><\/td><\/tr><tr><td><p><b>Sample Requirement<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">Amniotic Fluid (Plungerless syringe)<\/span><\/p><p><span style=\"font-weight: 400;\">Maternal blood in EDTA<\/span><\/p><p><span style=\"font-weight: 400;\">CVS<\/span><\/p><p><span style=\"font-weight: 400;\">Heparinized Blood<\/span><\/p><p><span style=\"font-weight: 400;\">Abortus Tissue\u00a0<\/span><\/p><p>Cord Blood (Cordocentesis)<\/p><\/td><\/tr><tr><td><p><b>Turnaround Time (TAT)<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">3-4 weeks (Amniocentesis)<\/span><\/p><p><span style=\"font-weight: 400;\">2-3 weeks (CVS and Abortus)<\/span><\/p><p><span style=\"font-weight: 400;\">15 days (Peripheral Blood)<\/span><\/p><\/td><\/tr><\/tbody><\/table><p>\u00a0<\/p><p><strong>Rapid Aneuploidy FISH<\/strong><\/p><p>Rapid Aneuploidy FISH is routinely recommended and performed at our center, providing rapid detection of common chromosomal aneuploidies in amniotic fluid and CVS specimens.<\/p><table><tbody><tr><td><p><b>Feature<\/b><\/p><\/td><td><p><b>Details<\/b><\/p><\/td><\/tr><tr><td><p><b>Method<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">\u00a0FISH<\/span><\/p><\/td><\/tr><tr><td><p><b>Coverage<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">Analysis of chromosomes 13, 18, 21, X, and Y<\/span><\/p><\/td><\/tr><tr><td><p><b>Sample Requirement<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">Fetal Blood<\/span><\/p><p><span style=\"font-weight: 400;\">CVS<\/span><\/p><p><span style=\"font-weight: 400;\">Amniotic Fluid<\/span><\/p><\/td><\/tr><tr><td><p><b>Turnaround Time (TAT)<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">3-5 days<\/span><\/p><\/td><\/tr><\/tbody><\/table><p>\u00a0<\/p><p><b>Molecular Karyotyping\u00a0<\/b><\/p><p>Molecular karyotyping enables the detection of chromosomal imbalances, including microdeletions and microduplications, that cannot be identified using conventional cytogenetic methods.<\/p><table><tbody><tr><td><p><b>Feature<\/b><\/p><\/td><td><p><b>Details<\/b><\/p><\/td><\/tr><tr><td><p><b>Method<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">Chromosomal Microarray Analysis (aCGH \/ SNP-array)<\/span><\/p><\/td><\/tr><tr><td><p><b>Coverage<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">CNV, del\/dup, LOH<\/span><\/p><\/td><\/tr><tr><td><p><b>Sample Requirement<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">Fetal Blood<\/span><\/p><p><span style=\"font-weight: 400;\">CVS<\/span><\/p><p><span style=\"font-weight: 400;\">Amniotic Fluid<\/span><\/p><p>Cord Blood (Cordocentesis)<\/p><p><span style=\"font-weight: 400;\">Heparinized Blood<\/span><\/p><\/td><\/tr><tr><td><p><b>Turnaround Time (TAT)<\/b><\/p><\/td><td><p><span style=\"font-weight: 400;\">2-3 weeks<\/span><\/p><\/td><\/tr><\/tbody><\/table><p><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">Maternal blood must be submitted alongside prenatal samples to exclude Maternal Cell Contamination. <br \/>*<\/span><span style=\"font-weight: 400;\">For a detailed sample collection, please contact our team.<\/span><\/p>\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 Chromosomal Alterations From Uncertainty to Clarity in Prenatal Diagnosis Chromosomal [&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-12605","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12605","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=12605"}],"version-history":[{"count":22,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12605\/revisions"}],"predecessor-version":[{"id":20831,"href":"https:\/\/nesiller.com\/en\/wp-json\/wp\/v2\/pages\/12605\/revisions\/20831"}],"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=12605"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}