{"id":27030,"date":"2025-06-24T15:38:12","date_gmt":"2025-06-24T12:38:12","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/qf-pcr-produs-de-conceptie-detectie-rapida-a-aneuploidiilor-cromozomilor-13-18-21-x-y\/"},"modified":"2026-06-16T11:37:11","modified_gmt":"2026-06-16T08:37:11","slug":"qf-pcr-produs-de-conceptie-detectie-rapida-a-aneuploidiilor-cromozomilor-13-18-21-x-y","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/qf-pcr-produs-de-conceptie-detectie-rapida-a-aneuploidiilor-cromozomilor-13-18-21-x-y\/","title":{"rendered":"QF-PCR produs de conceptie &#8211; detectie rapida a aneuploidiilor cromozomilor 13, 18, 21, X, Y"},"content":{"rendered":"<p>Testul QF-PCR este o metod\u0103 molecular\u0103 rapid\u0103 de diagnostic citogenetic, utilizat\u0103 pentru identificarea aneuploidiilor cromozomiale frecvente \u00een materialul provenit din avort spontan sau produs de concep\u021bie.<\/p>\n<p>Analiza detecteaz\u0103 varia\u021bii ale num\u0103rului de cromozomi prin cuantificarea fluorescent\u0103 a markerilor STR (Short Tandem Repeats), oferind rezultate rapide privind:<\/p>\n<ul>\n<li>trisomia 21 (sindrom Down)<\/li>\n<li>trisomia 18 (sindrom Edwards)<\/li>\n<li>trisomia 13 (sindrom Patau)<\/li>\n<li>anomalii ale cromozomilor sexuali (Turner, Klinefelter etc.)<\/li>\n<\/ul>\n<p>Este un test util \u00een evaluarea cauzelor genetice ale pierderilor de sarcin\u0103.<\/p>\n<h3>Afec\u021biuni sau riscuri genetice investigate:<\/h3>\n<ul>\n<li>Trisomia 21 (sindrom Down);<\/li>\n<li>Trisomia 18 (sindrom Edwards);<\/li>\n<li>Trisomia 13 (sindrom Patau);<\/li>\n<li>Monosomia X (sindrom Turner);<\/li>\n<li>Sindrom Klinefelter (XXY) \u0219i alte aneuploidii ale cromozomilor sexuali;<\/li>\n<li>Alte anomalii numerice ale cromozomilor 13, 18, 21, X \u0219i Y.<\/li>\n<\/ul>\n<h3>Cui se adreseaz\u0103:<\/h3>\n<p>Medicilor ginecologi, speciali\u0219tilor \u00een medicin\u0103 materno-fetal\u0103, geneticienilor medicali \u0219i laboratoarelor de genetic\u0103 implicate \u00een investigarea cauzelor genetice ale avortului spontan sau sarcinilor oprite \u00een evolu\u021bie.<\/p>\n<h3>Metodologie de testare:<\/h3>\n<p>QF-PCR (Quantitative Fluorescent PCR) utiliz\u00e2nd markeri STR specifici pentru cromozomii 13, 18, 21, X \u0219i Y.<\/p>\n<h3>Analiza se efectueaz\u0103 pe ADN extras din:<\/h3>\n<ul>\n<li>\u021besut de produs de concep\u021bie<\/li>\n<li>material abortiv (vilozit\u0103\u021bi coriale fetale)<\/li>\n<\/ul>\n<p>Metoda permite detectarea rapid\u0103 a dezechilibrelor cromozomiale numerice prin analiza intensit\u0103\u021bii fluorescente a alelelor.<\/p>\n<h3>Beneficii \u0219i importan\u021b\u0103 clinic\u0103:<\/h3>\n<ul>\n<li>Poate identifica rapid unele dintre cele mai frecvente cauze genetice ale avortului spontan;<\/li>\n<li>Detecteaz\u0103 cele mai comune aneuploidii fetale;<\/li>\n<li>Ajut\u0103 la consilierea genetic\u0103 a cuplurilor dup\u0103 pierdere de sarcin\u0103;<\/li>\n<li>Reduce timpul de a\u0219teptare comparativ cu cariotipul clasic;<\/li>\n<li>Poate orienta necesitatea unor investiga\u021bii reproductive suplimentare.<\/li>\n<\/ul>\n<h3>Particularit\u0103\u021bi \u0219i limit\u0103ri:<\/h3>\n<ul>\n<li>Detecteaz\u0103 doar aneuploidiile cromozomilor 13, 18, 21, X \u0219i Y;<\/li>\n<li>Nu identific\u0103 anomalii structurale (dele\u021bii\/duplica\u021bii submicroscopice);<\/li>\n<li>Nu detecteaz\u0103 mozaicism \u00een toate cazurile;<\/li>\n<li>Nu \u00eenlocuie\u0219te cariotipul sau microarray-ul genomic;<\/li>\n<li>Necesit\u0103 prob\u0103 fetal\u0103 adecvat\u0103, f\u0103r\u0103 contaminare matern\u0103 semnificativ\u0103.<\/li>\n<\/ul>\n<h3>Tip prob\u0103:<\/h3>\n<ul>\n<li>\u021aesut produs de concep\u021bie (avort spontan)<\/li>\n<li>Vilozit\u0103\u021bi coriale din material abortiv<\/li>\n<\/ul>\n<h3>Recoltare:<\/h3>\n<p>Proba se colecteaz\u0103 steril din produsul de concep\u021bie, preferabil cu identificarea \u021besutului fetal (vilozit\u0103\u021bi coriale). Este esen\u021bial\u0103 evitarea contamin\u0103rii cu \u021besut matern pentru acurate\u021bea rezultatului.<\/p>\n<h3>Condi\u021bii:<\/h3>\n<p>Calitatea \u0219i puritatea ADN-ului fetal sunt critice. Prezen\u021ba contamin\u0103rii materne sau degradarea \u021besutului poate limita interpretarea rezultatelor sau necesita teste suplimentare.<\/p>\n<h3>Denumiri alternative:<\/h3>\n<p>QF-PCR prenatal\/post-avort;<\/p>\n<p>Test rapid aneuploidii fetale;<\/p>\n<p>Analiz\u0103 genetic\u0103 produs de concep\u021bie;<\/p>\n<p>Detec\u021bie rapid\u0103 a trisomiilor 13, 18, 21 \u0219i a anomaliilor gonozomiale.<\/p>\n<h3>Analize asociate recomandate:<\/h3>\n<ul>\n<li>Microarray genomic (CentoArray Cyto) pentru anomalii submicroscopice;<\/li>\n<li>Cariotip clasic din produs de concep\u021bie;<\/li>\n<li>Testare parental\u0103 genetic\u0103 pentru transloca\u021bii echilibrate;<\/li>\n<li>Analize de trombofilie \u0219i factori imunologici \u00een avort recurent;<\/li>\n<li>Consiliere genetic\u0103 reproductiv\u0103 post-eveniment;<\/li>\n<li>Testare genetic\u0103 extins\u0103 (WES) \u00een caz de pierderi recurente inexplicabile.<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Analiz\u0103 genetic\u0103 rapid\u0103 bazat\u0103 pe tehnica QF-PCR (Quantitative Fluorescent PCR), utilizat\u0103 pentru detectarea aneuploidiilor frecvente ale cromozomilor 13, 18, 21 \u0219i ale cromozomilor sexuali X \u0219i Y \u00een \u021besutul provenit din produsul de concep\u021bie.<\/p>\n","protected":false},"featured_media":27938,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3173,2876],"product_tag":[],"class_list":["post-27030","product","type-product","status-publish","has-post-thumbnail","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=\"Analiz\u0103 genetic\u0103 rapid\u0103 bazat\u0103 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