{"id":104971,"date":"2026-06-12T21:26:38","date_gmt":"2026-06-12T18:26:38","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize\/cultura-si-analiza-cromozomilor-din-vilozitati-coriale-cariotip-vilozitati-coriale\/"},"modified":"2026-07-20T11:21:28","modified_gmt":"2026-07-20T08:21:28","slug":"cultura-si-analiza-cromozomilor-din-vilozitati-coriale-cariotip-vilozitati-coriale","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/cultura-si-analiza-cromozomilor-din-vilozitati-coriale-cariotip-vilozitati-coriale\/","title":{"rendered":"Cultura si analiza cromozomilor din vilozitati coriale (cariotip vilozitati coriale)"},"content":{"rendered":"<p>Cariotipul reprezint\u0103 <strong>imaginea complet\u0103 a setului de cromozomi<\/strong> ai f\u0103tului, ob\u021binut\u0103 prin tehnici citogenetice. Analiza poate identifica:<\/p>\n<\/p>\n<p><strong>1.Anomalii numerice ale cromozomilor (aneuploidii)<\/strong><\/p>\n<\/p>\n<ul>\n<li>trisomii: prezen\u021ba unui cromozom suplimentar (ex.: Trisomia 21 \u2013 Sindromul Down);<\/li>\n<li>monosomii: lipsa unui cromozom (ex.: Monosomia X \u2013 Sindromul Turner);<\/li>\n<li>exemple: 47,XXY (Sindromul Klinefelter).<\/li>\n<\/ul>\n<p><strong>2.Anomalii structurale ale cromozomilor<\/strong><\/p>\n<\/p>\n<ul>\n<li>transloca\u021bii (reciproc\u0103 sau robertsonian\u0103, echilibrate sau dezechilibrate);<\/li>\n<li>dele\u021bii, duplicatii, inversii sau inser\u021bii.<\/li>\n<\/ul>\n<p><strong>3.Rearanjamente cromozomiale complexe<\/strong><\/p>\n<\/p>\n<ul>\n<li>asociate cu risc de malforma\u021bii congenitale, avorturi recurente sau transmitere ereditar\u0103.<\/li>\n<\/ul>\n<p><strong>Metodologie de testare<\/strong><\/p>\n<\/p>\n<p> Analiza prenatal\u0103 se realizeaz\u0103 prin tehnici citogenetice, cu pa\u0219i specifici:<\/p>\n<\/p>\n<ul>\n<li>recoltarea probei de lichid amniotic sau vilozit\u0103\u021bi coriale;<\/li>\n<li>izolarea celulelor fetale \u0219i cultivarea lor \u00een laborator;<\/li>\n<li>stimularea diviziunii celulare \u0219i oprirea celulelor \u00een metafaz\u0103;<\/li>\n<li>colorarea cromozomilor prin tehnica de benzi (G-banding);<\/li>\n<li>analiza microscopic\u0103 \u0219i aranjarea cromozomilor \u00een perechi pentru identificarea eventualelor anomalii numerice sau structurale.<\/li>\n<\/ul>\n<p><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<\/p>\n<p> Analiza cromozomial\u0103 prenatal\u0103 este recomandat\u0103 \u00een urm\u0103toarele situa\u021bii:<\/p>\n<\/p>\n<ul>\n<li>v\u00e2rsta matern\u0103 de peste 35 de ani sau risc crescut de anomalii cromozomiale;<\/li>\n<li>antecedente de sarcini cu anomalii cromozomiale sau avorturi spontane recurente;<\/li>\n<li>malforma\u021bii congenitale detectate ecografic;<\/li>\n<li>familie cu istoric de anomalii cromozomiale;<\/li>\n<li>screening prenatal complementar \u00een cazul testelor genetice non-invazive (NIPT) cu rezultate suspecte.<\/li>\n<\/ul>\n<p><strong>C\u00e2nd NU se recomand\u0103 analiza cromozomial\u0103 prenatal\u0103:<\/strong><\/p>\n<\/p>\n<ul>\n<li>dac\u0103 se suspecteaz\u0103 o afec\u021biune genetic\u0103 submicroscopic\u0103 \u2192 se recomand\u0103 array-CGH;<\/li>\n<li>dac\u0103 se suspecteaz\u0103 boal\u0103 monogenic\u0103 \u2192 se recomand\u0103 secven\u021biere genetic\u0103;<\/li>\n<li>\u00een boli mitocondriale \u2192 se analizeaz\u0103 ADN-ul mitocondrial.<\/li>\n<\/ul>\n<p><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri:<\/strong><\/p>\n<\/p>\n<ul>\n<li>analiza cromozomial\u0103 detecteaz\u0103 anomalii mari (cromozomi \u00een plus, lips\u0103 sau rearanj\u0103ri vizibile);<\/li>\n<li>modific\u0103rile genetice subtile (muta\u021bii punctiforme, boli monogenice sau mitocondriale) necesit\u0103 teste genetice suplimentare.<\/li>\n<\/ul>\n<p><strong>Tip prob\u0103: <\/strong><\/p>\n<\/p>\n<ul>\n<li><strong>lichid amniotic:<\/strong> recoltat prin amniocentez\u0103;<\/li>\n<li><strong>vilozit\u0103\u021bi coriale:<\/strong> recoltate prin biopsie corial\u0103 (CVS).<\/li>\n<\/ul>\n<p><strong>Recoltare \u0219i condi\u021bii:<\/strong><\/p>\n<\/p>\n<ul>\n<li>nu necesit\u0103 post alimentar;<\/li>\n<li>recoltarea se face la indica\u021bia medicului, \u00een centre dedicate, de c\u0103tre personal medical specializat.<\/li>\n<\/ul>\n<p>Pentru interpretarea rezultatelor de genetic\u0103, v\u0103 pute\u021bi adresa speciali\u0219tilor no\u0219tri. Ei v\u0103 pot ghida \u0219i v\u0103 pot oferi informa\u021bii suplimentare despre testele genetice din oferta noastr\u0103. Consultul genetic se poate programa at\u00e2t \u00eenainte, c\u00e2t \u0219i dup\u0103 efectuarea testului. Consultul genetic de dup\u0103 test este <strong>GRATUIT<\/strong> \u0219i este destinat interpret\u0103rii rezultatelor \u0219i stabilirii indica\u021biilor terapeutice.<\/p>\n<\/p>\n<p><strong>E-mail:<\/strong> <strong><a href=\"mailto:consult.genetic@clinica-sante.ro\" rel=\"noopener noreferrer\" target=\"_blank\">consult.genetic@clinica-sante.ro<\/a> <\/strong><\/p>\n<\/p>\n<p><strong>Telefon: <\/strong>0773.975.894 <\/p>\n<\/p>\n<p><strong>Program:<\/strong> Luni\u2013Vineri<\/p>\n<\/p>\n<p><strong>Orele:<\/strong> 8:00\u201316:30<\/p>\n<\/p>\n<p><strong>Call Center:<\/strong> *8787<\/p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Aceast\u0103 investiga\u021bie reprezint\u0103 o metod\u0103 citogenetic\u0103 avansat\u0103 care analizeaz\u0103 structura \u0219i num\u0103rul cromozomilor \u00een celulele ob\u021binute din <strong>lichid amniotic sau vilozit\u0103\u021bi coriale<\/strong>, cu scopul evalu\u0103ri genetice prenatale.<\/p>\n<\/p>\n<p>Genomul uman este organizat \u00een <strong>23 de perechi de cromozomi<\/strong>: 22 perechi de autozomi \u0219i o pereche de cromozomi sexuali (XX la fetu\u0219i feminini, XY la fetu\u0219i masculini).<\/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-104971","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 5.0.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Aceast\u0103 investiga\u021bie reprezint\u0103 o metod\u0103 citogenetic\u0103 avansat\u0103 care analizeaz\u0103 structura \u0219i num\u0103rul cromozomilor \u00een celulele ob\u021binute din lichid amniotic sau vilozit\u0103\u021bi coriale, cu scopul 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