{"id":27657,"date":"2025-06-24T15:47:33","date_gmt":"2025-06-24T13:47:33","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/arraycgh-prenatal-60k-cytoarray-prenatal-agilent-60k\/"},"modified":"2026-02-27T18:04:35","modified_gmt":"2026-02-27T16:04:35","slug":"arraycgh-prenatal-60k-cytoarray-prenatal-agilent-60k","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/arraycgh-prenatal-60k-cytoarray-prenatal-agilent-60k\/","title":{"rendered":"ArrayCGH prenatal &#8211; 60K &#8211; Cytoarray Prenatal &#8211; Agilent 60K"},"content":{"rendered":"<p><strong>ArrayCGH Prenatal 60K<\/strong> utilizeaz\u0103 o matrice cu 60.000 de sonde distribuite pe \u00eentregul genom. Testul detecteaz\u0103 varia\u021bii ale num\u0103rului de copii (CNV), inclusiv microdele\u021bii \u0219i duplica\u021bii submicroscopice. Este recomandat atunci c\u00e2nd cariotipul conven\u021bional este normal sau insuficient pentru explicarea anomaliilor detectate ecografic.<\/p>\n<\/p>\n<p><strong style=\"color: #ff9900\">Afec\u021biuni sau simptome asociate<\/strong><\/p>\n<\/p>\n<ul>\n<li>Anomalii ecografice fetale<\/li>\n<li>Suspiciune de sindrom genetic sau anomalii cromozomiale subtile<\/li>\n<li>Avorturi spontane recurente cu cauz\u0103 genetic\u0103 posibil\u0103<\/li>\n<li>Sarcini cu istoric de anomalii cromozomiale<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Cui se adreseaz\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>Femeilor \u00eens\u0103rcinate care au indicii ecografice sau istoric de risc genetic<\/li>\n<li>Pacientelor care doresc evaluarea detaliat\u0103 a genomului fetal pentru microdele\u021bii \/ duplica\u021bii subtile<\/li>\n<li>\u00cen contextul consilierii genetice prenatale pentru planificarea sarcinilor viitoare<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Metodologie de testare<\/strong><\/p>\n<\/p>\n<ul>\n<li>Hibridizare genomic\u0103 comparativ\u0103 (ArrayCGH) pe matrice 60K Agilent<\/li>\n<li>Compararea ADN fetal cu ADN de control<\/li>\n<li>Detectarea microdele\u021biilor \u0219i microduplica\u021biilor la rezolu\u021bie ~7.1 kb<\/li>\n<li>Software specializat pentru analiza CNV \u0219i raportarea rezultatelor<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Beneficii \u0219i importan\u021ba clinic\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>Detecteaz\u0103 anomalii cromozomiale subtile nedetectabile prin cariotip conven\u021bional<\/li>\n<li>Ofer\u0103 suport pentru decizii clinice \u0219i consiliere genetic\u0103 prenatal\u0103<\/li>\n<li>Permite identificarea cauzelor genetice ale anomaliilor detectate ecografic<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<\/p>\n<ul>\n<li>Rezultatele depind de calitatea probei \u0219i de gradul de contaminare cu s\u00e2nge matern<\/li>\n<li>Dac\u0103 proba prezint\u0103 contaminare mare cu s\u00e2nge matern, rezultatul nu poate fi emis; \u00een acest caz se va percepe plata testului de evaluare a contamin\u0103rii materne<\/li>\n<li>Nu detecteaz\u0103 muta\u021bii punctiforme sau anomalii monogenice<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Tip prob\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>Lichid amniotic<\/li>\n<li>Vilozit\u0103\u021bi coriale<\/li>\n<li>S\u00e2nge fetal<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Condi\u021bii pentru recoltare<\/strong><\/p>\n<\/p>\n<ul>\n<li>Recoltare conform protocoalelor prenatale, evit\u00e2nd contaminarea matern\u0103<\/li>\n<li>Proba trebuie prelucrat\u0103 rapid \u0219i trimis\u0103 la laborator \u00een condi\u021bii de siguran\u021b\u0103<\/li>\n<li>Este recomandat\u0103 recoltarea imediat dup\u0103 detectarea indica\u021biei clinice<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">Analize asociate recomandate<\/strong><\/p>\n<\/p>\n<ul>\n<li>Consult genetic prenatal pentru interpretarea rezultatelor<\/li>\n<li>Teste complementare \u00een cazul identific\u0103rii unor CNV-uri relevante<\/li>\n<li>Confirmare prin metode ortogonale (FISH, MLPA) dac\u0103 este necesar<\/li>\n<\/ul><\/p>\n","protected":false},"excerpt":{"rendered":"<p><strong>ArrayCGH Prenatal 60K<\/strong> este o analiz\u0103 genomic\u0103 ce utilizeaz\u0103 hibridizare genomic\u0103 comparativ\u0103 (ArrayCGH) pentru detectarea anomaliilor cromozomiale submicroscopice \u00een sarcinile \u00een curs. Analiza permite identificarea microdele\u021biilor \u0219i microduplica\u021biilor, oferind informa\u021bii suplimentare fa\u021b\u0103 de cariotipul conven\u021bional.<\/p>\n<\/p>\n<p><strong style=\"color: #ff9900\">Gene analizate<\/strong><\/p>\n<\/p>\n<p>Testul investigheaz\u0103 \u00eentregul genom, cu accent pe regiunile cel mai frecvent implicate \u00een patologie, incluz\u00e2nd cromozomii autozomali \u0219i regiuni critice pentru anomalii prenatale.<\/p><\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3173,2876],"product_tag":[],"class_list":["post-27657","product","type-product","status-publish","product_cat-analize","product_cat-genetica-in-sarcina","product_cat-serviciu-laborator","first","instock","sale","virtual","purchasable","product-type-simple"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.10 - aioseo.com -->\n\t<meta name=\"description\" content=\"ArrayCGH Prenatal 60K este o analiz\u0103 genomic\u0103 ce utilizeaz\u0103 hibridizare genomic\u0103 comparativ\u0103 (ArrayCGH) pentru detectarea anomaliilor cromozomiale submicroscopice \u00een sarcinile \u00een curs. Analiza permite identificarea microdele\u021biilor \u0219i microduplica\u021biilor, oferind informa\u021bii suplimentare fa\u021b\u0103 de cariotipul conven\u021bional.Gene analizateTestul investigheaz\u0103 \u00eentregul genom, cu accent pe regiunile cel mai frecvent implicate \u00een patologie, incluz\u00e2nd cromozomii autozomali \u0219i regiuni critice pentru anomalii prenatale.\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<link rel=\"canonical\" href=\"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/arraycgh-prenatal-60k-cytoarray-prenatal-agilent-60k\/\" \/>\n\t<meta name=\"generator\" content=\"All in One SEO Pro (AIOSEO) 4.9.10\" \/>\n\t\t<meta property=\"og:locale\" content=\"ro_RO\" \/>\n\t\t<meta property=\"og:site_name\" content=\"Clinica Sante - Laborator de Analize Medicale - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:type\" content=\"article\" \/>\n\t\t<meta property=\"og:title\" content=\"ArrayCGH prenatal \u2013 60K \u2013 Cytoarray Prenatal \u2013 Agilent 60K - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"ArrayCGH Prenatal 60K este o analiz\u0103 genomic\u0103 ce utilizeaz\u0103 hibridizare genomic\u0103 comparativ\u0103 (ArrayCGH) pentru detectarea anomaliilor cromozomiale submicroscopice \u00een sarcinile \u00een curs. Analiza permite identificarea microdele\u021biilor \u0219i microduplica\u021biilor, oferind informa\u021bii suplimentare fa\u021b\u0103 de cariotipul conven\u021bional.Gene analizateTestul investigheaz\u0103 \u00eentregul genom, cu accent pe regiunile cel mai frecvent implicate \u00een patologie, incluz\u00e2nd cromozomii autozomali \u0219i regiuni critice pentru anomalii prenatale.\" \/>\n\t\t<meta property=\"og:url\" content=\"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/arraycgh-prenatal-60k-cytoarray-prenatal-agilent-60k\/\" \/>\n\t\t<meta property=\"article:published_time\" content=\"2025-06-24T13:47:33+00:00\" \/>\n\t\t<meta property=\"article:modified_time\" content=\"2026-02-27T16:04:35+00:00\" \/>\n\t\t<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n\t\t<meta name=\"twitter:title\" content=\"ArrayCGH prenatal \u2013 60K \u2013 Cytoarray Prenatal \u2013 Agilent 60K - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta name=\"twitter:description\" content=\"ArrayCGH Prenatal 60K este o analiz\u0103 genomic\u0103 ce utilizeaz\u0103 hibridizare genomic\u0103 comparativ\u0103 (ArrayCGH) pentru detectarea anomaliilor cromozomiale submicroscopice \u00een sarcinile \u00een curs. 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