{"id":27400,"date":"2025-06-24T14:58:57","date_gmt":"2025-06-24T12:58:57","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/testare-non-invaziva-produs-conceptie-ngs\/"},"modified":"2026-02-27T18:02:07","modified_gmt":"2026-02-27T16:02:07","slug":"testare-non-invaziva-produs-conceptie-ngs","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/testare-non-invaziva-produs-conceptie-ngs\/","title":{"rendered":"Testare non-invaziva Produs conceptie NGS"},"content":{"rendered":"<p>Testare non-invaziv\u0103 Produs Concep\u021bie utilizeaz\u0103 ADN fetal liber \u00een s\u00e2ngele matern pentru a evalua anomalii cromozomiale care pot cauza oprirea dezvolt\u0103rii sarcinii. Este un test non-invaziv, sigur, care elimin\u0103 riscul de contaminare matern\u0103 \u0219i ofer\u0103 rezultate rapide, precise \u0219i reproductibile.<\/p>\n<\/p>\n<p><strong>Afec\u021biuni sau simptome asociate<\/strong><\/p>\n<\/p>\n<ul>\n<li>Sarcin\u0103 oprit\u0103 din evolu\u021bie<\/li>\n<li>Lipsa b\u0103t\u0103ilor inimii fetale detectat\u0103 ecografic<\/li>\n<li>Sarcini cu ou clar sau sarcini molare<\/li>\n<li>Avort spontan \u00een desf\u0103\u0219urare<\/li>\n<\/ul>\n<p><strong>Cui se adreseaz\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>Pacientelor cu pierdere spontan\u0103 a sarcinii, fie \u00eentrerupt\u0103, fie \u00een curs de desf\u0103\u0219urare<\/li>\n<li>Pacientelor cu suspiciune de cauz\u0103 genetic\u0103 a pierderii sarcinii<\/li>\n<li>Pacientelor care planific\u0103 o sarcin\u0103 viitoare \u0219i doresc evaluarea riscului genetic<\/li>\n<\/ul>\n<p><strong>Metodologie de testare<\/strong><\/p>\n<\/p>\n<ul>\n<li>Testare non-invaziv\u0103 din s\u00e2nge matern<\/li>\n<li>Tehnologie Next-Generation Sequencing (NGS) pentru analiza ADN-ului fetal<\/li>\n<li>Detectarea CNV-urilor &gt;7 Mb \u0219i a aneuploidiilor par\u021biale \/ transloca\u021biilor neechilibrate<\/li>\n<\/ul>\n<p><strong>Beneficii \u0219i importan\u021ba clinic\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>Permite identificarea cauzei genetice a avortului spontan, superioar\u0103 test\u0103rii citogenetice tradi\u021bionale<\/li>\n<li>Test sigur, realizat din s\u00e2nge matern, f\u0103r\u0103 risc pentru pacient\u0103 sau f\u0103t<\/li>\n<li>Cre\u0219te probabilitatea ob\u021binerii unui rezultat relevant, reduc\u00e2nd riscul de contaminare matern\u0103<\/li>\n<li>Ofer\u0103 suport pentru consiliere genetic\u0103 \u0219i planificarea sarcinilor viitoare<\/li>\n<\/ul>\n<p><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<\/p>\n<ul>\n<li>Testul se recomand\u0103 doar \u00een sarcini oprite din evolu\u021bie, \u00eenainte de chiuretaj<\/li>\n<li>Nu este indicat pentru detectarea altor tipuri de muta\u021bii genetice monogenice<\/li>\n<li>Rezultatul reflect\u0103 anomaliile cromozomiale fetale detectabile \u00een s\u00e2ngele matern la momentul recolt\u0103rii<\/li>\n<\/ul>\n<p><strong>Tip prob\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>S\u00e2nge matern recoltat pe vacutainer Streck<\/li>\n<\/ul>\n<p><strong>Condi\u021bii pentru recoltare<\/strong><\/p>\n<\/p>\n<ul>\n<li>Prescrip\u021bie medical\u0103 obligatorie<\/li>\n<li>Recoltarea trebuie f\u0103cut\u0103 c\u00e2t mai cur\u00e2nd dup\u0103 confirmarea opririi sarcinii<\/li>\n<li>Recoltarea obligatoriu \u00eenainte de chiuretaj<\/li>\n<li>Rezultatul este disponibil \u00een <strong>7 zile lucr\u0103toare<\/strong> de la primirea probei \u00een laborator<\/li>\n<\/ul>\n<p><strong>Analize asociate recomandate<\/strong><\/p>\n<\/p>\n<ul>\n<li>Consult genetic post-test pentru interpretarea rezultatelor \u0219i consiliere reproductiv\u0103<\/li>\n<li>Analize complementare pentru evaluarea factorilor materni sau reproductivi<\/li>\n<li>Teste genetice pentru ambii p\u0103rin\u021bi \u00een cazul recuren\u021bei pierderilor de sarcin\u0103<\/li>\n<\/ul><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Testare non-invaziv\u0103 Produs Concep\u021bie este un screening genetic avansat, non-invaziv, realizat prin tehnologie NGS, destinat identific\u0103rii cauzelor genetice posibile ale pierderilor spontane de sarcin\u0103. Permite detectarea anomaliilor cromozomiale fetale care pot determina avort spontan, furniz\u00e2nd informa\u021bii esen\u021biale pentru consilierea genetic\u0103 reproductiv\u0103.<\/p>\n<\/p>\n<p><strong>Gene analizate<\/strong><\/p>\n<\/p>\n<p>Testul analizeaz\u0103 cromozomii autozomali, identific\u00e2nd:<\/p>\n<\/p>\n<ul>\n<li>Dele\u021bii \u0219i duplica\u021bii (CNVs) &gt;7 Mb<\/li>\n<li>Aneuploidii cromozomiale par\u021biale \u0219i transloca\u021bii neechilibrate<\/li>\n<\/ul>\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-27400","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 5.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Testare non-invaziv\u0103 Produs Concep\u021bie este un screening genetic avansat, non-invaziv, realizat prin tehnologie NGS, destinat identific\u0103rii cauzelor genetice posibile ale pierderilor spontane de sarcin\u0103. Permite detectarea anomaliilor cromozomiale fetale care pot determina avort spontan, furniz\u00e2nd informa\u021bii esen\u021biale pentru consilierea genetic\u0103 reproductiv\u0103.Gene analizateTestul analizeaz\u0103 cromozomii autozomali, identific\u00e2nd:Dele\u021bii \u0219i duplica\u021bii (CNVs) &gt;7 MbAneuploidii cromozomiale par\u021biale \u0219i transloca\u021bii neechilibrate\" \/>\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\/testare-non-invaziva-produs-conceptie-ngs\/\" \/>\n\t<meta name=\"generator\" content=\"All in One SEO Pro (AIOSEO) 5.0.1\" \/>\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=\"Testare non-invaziva Produs conceptie NGS - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"Testare non-invaziv\u0103 Produs Concep\u021bie este un screening genetic avansat, non-invaziv, realizat prin tehnologie NGS, destinat identific\u0103rii cauzelor genetice posibile ale pierderilor spontane de sarcin\u0103. Permite detectarea anomaliilor cromozomiale fetale care pot determina avort spontan, furniz\u00e2nd informa\u021bii esen\u021biale pentru consilierea genetic\u0103 reproductiv\u0103.Gene analizateTestul analizeaz\u0103 cromozomii autozomali, identific\u00e2nd:Dele\u021bii \u0219i duplica\u021bii (CNVs) &gt;7 MbAneuploidii cromozomiale par\u021biale \u0219i transloca\u021bii neechilibrate\" \/>\n\t\t<meta property=\"og:url\" content=\"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/testare-non-invaziva-produs-conceptie-ngs\/\" \/>\n\t\t<meta property=\"article:published_time\" content=\"2025-06-24T12:58:57+00:00\" \/>\n\t\t<meta property=\"article:modified_time\" content=\"2026-02-27T16:02:07+00:00\" \/>\n\t\t<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n\t\t<meta name=\"twitter:title\" content=\"Testare non-invaziva Produs conceptie NGS - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta name=\"twitter:description\" content=\"Testare non-invaziv\u0103 Produs Concep\u021bie este un screening genetic avansat, non-invaziv, realizat prin tehnologie NGS, destinat identific\u0103rii cauzelor genetice posibile ale pierderilor spontane de sarcin\u0103. 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