{"id":104970,"date":"2026-06-12T21:25:46","date_gmt":"2026-06-12T18:25:46","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize\/cultura-si-analiza-cromozomilor-din-sange-fetal-cariotip-sange-cordon-ombilical\/"},"modified":"2026-06-30T15:58:35","modified_gmt":"2026-06-30T12:58:35","slug":"cultura-si-analiza-cromozomilor-din-sange-fetal-cariotip-sange-cordon-ombilical","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/cultura-si-analiza-cromozomilor-din-sange-fetal-cariotip-sange-cordon-ombilical\/","title":{"rendered":"Cultura si analiza cromozomilor din sange fetal (cariotip sange cordon ombilical)"},"content":{"rendered":"<p>Analiza este indicat\u0103 \u00een evaluarea prenatal\u0103 a anomaliilor cromozomiale atunci c\u00e2nd este necesar\u0103 confirmarea unui diagnostic genetic fetal sau completarea investiga\u021biilor ecografice\/biologice sugestive.<\/p>\n<h3>Termen de execu\u021bie*<\/h3>\n<p>14\u201321 zile lucr\u0103toare (\u00een func\u021bie de rata de cre\u0219tere a culturii celulare)<\/p>\n<h3>Despre cariotipul din s\u00e2nge fetal (cordon ombilical)<\/h3>\n<p>S\u00e2ngele din cordonul ombilical con\u021bine limfocite fetale viabile, care pot fi cultivate in vitro pentru ob\u021binerea metafazelor necesare analizei cromozomiale.<\/p>\n<p>Testul utilizeaz\u0103 tehnica standard de <strong>citogenetic\u0103 conven\u021bional\u0103 (G-banding)<\/strong>, care permite vizualizarea cromozomilor la microscop \u0219i identificarea:<\/p>\n<ul>\n<li>aneuploidiilor (ex. trisomii, monosomii)<\/li>\n<li>dele\u021biilor \u0219i duplica\u021biilor mari<\/li>\n<li>transloca\u021biilor echilibrate sau dezechilibrate<\/li>\n<li>inversiilor cromozomiale<\/li>\n<li>mozaicismului cromozomial (\u00een anumite limite de detec\u021bie)<\/li>\n<\/ul>\n<p>Aceast\u0103 metod\u0103 ofer\u0103 o imagine global\u0103 a genomului fetal la nivel cromozomial, fiind considerat\u0103 standardul clasic \u00een citogenetica prenatal\u0103.<\/p>\n<h3>Afec\u021biuni sau indica\u021bii clinice asociate<\/h3>\n<h3>Testul este indicat \u00een:<\/h3>\n<ul>\n<li>suspiciune de anomalii cromozomiale fetale<\/li>\n<li>rezultate anormale la testele de screening prenatal (NIPT, dublu\/triplu test)<\/li>\n<li>anomalii ecografice fetale (malforma\u021bii structurale)<\/li>\n<li>restric\u021bie de cre\u0219tere intrauterin\u0103 (IUGR)<\/li>\n<li>translucen\u021b\u0103 nucal\u0103 crescut\u0103<\/li>\n<li>suspiciune de sindrom Down, Edwards, Patau<\/li>\n<li>suspiciune de mozaicism cromozomial<\/li>\n<li>istoric familial de anomalii cromozomiale<\/li>\n<li>sarcini cu risc genetic crescut<\/li>\n<li>confirmarea unui diagnostic prenatal incert<\/li>\n<\/ul>\n<h3>Cui se adreseaz\u0103<\/h3>\n<ul>\n<li>sarcinilor cu suspiciune de anomalii genetice fetale<\/li>\n<li>cazurilor cu ecografie fetal\u0103 modificat\u0103<\/li>\n<li>gravidelor cu rezultate NIPT pozitive sau neconcludente<\/li>\n<li>sarcinilor cu istoric de anomalii cromozomiale<\/li>\n<li>cazurilor \u00een care este necesar\u0103 confirmarea citogenetic\u0103 direct\u0103 fetal\u0103<\/li>\n<li>recomandare de c\u0103tre medicul specialist \u00een medicin\u0103 materno-fetal\u0103<\/li>\n<\/ul>\n<h3>Metodologie de testare<\/h3>\n<ul>\n<li>recoltare s\u00e2nge fetal din cordon ombilical (cordocentez\u0103)<\/li>\n<li>recoltare \u00een tub cu <strong>heparin\u0103 sodic\u0103<\/strong><\/li>\n<li>separarea limfocitelor fetale din s\u00e2ngele integral<\/li>\n<li>cultur\u0103 celular\u0103 in vitro (mitogen-stimulat\u0103)<\/li>\n<li>blocare \u00een metafaz\u0103 a diviziunii celulare<\/li>\n<li>bandare cromozomial\u0103 GTG (G-banding)<\/li>\n<li>analiz\u0103 microscopic\u0103 a cromozomilor<\/li>\n<li>interpretare citogenetic\u0103 conform ISCN<\/li>\n<li>raportare cariotip complet (46,XX \/ 46,XY sau anomalii structurale\/numerice)<\/li>\n<\/ul>\n<h3>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/h3>\n<ul>\n<li>ofer\u0103 diagnosticul complet al anomaliilor cromozomiale fetale<\/li>\n<li>confirm\u0103 sau infirm\u0103 suspiciuni ecografice sau de screening prenatal<\/li>\n<li>detecteaz\u0103 anomalii numerice \u0219i structurale majore<\/li>\n<li>permite consilierea genetic\u0103 prenatal\u0103 precis\u0103<\/li>\n<li>contribuie la decizii obstetricale informate<\/li>\n<li>poate reduce necesitatea unor investiga\u021bii suplimentare invazive<\/li>\n<li>r\u0103m\u00e2ne standardul de referin\u021b\u0103 \u00een citogenetica prenatal\u0103 clasic\u0103<\/li>\n<\/ul>\n<h3>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/h3>\n<ul>\n<li>necesit\u0103 cultur\u0103 celular\u0103 (timp de execu\u021bie mai mare)<\/li>\n<li>nu detecteaz\u0103 microdele\u021bii\/microduplica\u021bii sub rezolu\u021bia cariotipului<\/li>\n<li>nu identific\u0103 muta\u021bii punctiforme (SNV) sau boli monogenice<\/li>\n<li>rezolu\u021bia este limitat\u0103 (~5\u201310 Mb, \u00een func\u021bie de laborator)<\/li>\n<li>poate fi afectat de e\u0219ec de cultur\u0103 celular\u0103 (rar)<\/li>\n<li>mozaicismul poate fi subestimat \u00een unele cazuri<\/li>\n<li>necesit\u0103 confirmare prin tehnici moleculare (QF-PCR, microarray, NGS) \u00een cazuri selectate<\/li>\n<\/ul>\n<h3>Tip prob\u0103 \u0219i condi\u021bii de recoltare<\/h3>\n<h3>Prob\u0103 necesar\u0103:<\/h3>\n<ul>\n<li>s\u00e2nge fetal din cordon ombilical (cordocentez\u0103)<\/li>\n<\/ul>\n<h3>Tub de recoltare:<\/h3>\n<ul>\n<li>heparin\u0103 sodic\u0103<\/li>\n<\/ul>\n<h3>Condi\u021bii de recoltare:s<\/h3>\n<ul>\n<li>recoltare efectuat\u0103 de medic specialist \u00een medicin\u0103 materno-fetal\u0103<\/li>\n<li>manipulare rapid\u0103 pentru men\u021binerea viabilit\u0103\u021bii celulare<\/li>\n<li>transport la temperatur\u0103 controlat\u0103 (18\u201325\u00b0C, evit\u00e2nd refrigerarea excesiv\u0103)<\/li>\n<li>e\u0219antion proasp\u0103t pentru cultur\u0103 celular\u0103 optim\u0103<\/li>\n<li>formular de consim\u021b\u0103m\u00e2nt informat obligatoriu<\/li>\n<\/ul>\n<h3>Analize asociate recomandate<\/h3>\n<ul>\n<li><strong>QF-PCR pentru aneuploidii (13, 18, 21, X\/Y)<\/strong> \u2013 rezultat rapid prenatal<\/li>\n<li><strong>Microarray CGH fetal<\/strong> \u2013 detec\u021bie microdele\u021bii\/microduplica\u021bii<\/li>\n<li><strong>NGS panou boli monogenice fetale<\/strong> \u2013 \u00een suspiciuni complexe<\/li>\n<li><strong>NIPT (screening prenatal non-invaziv)<\/strong> \u2013 evaluare ini\u021bial\u0103<\/li>\n<li><strong>Ecografie morfologic\u0103<\/strong> fetal\u0103 detaliat\u0103<\/li>\n<li><strong>Consiliere <\/strong>genetic\u0103 prenatal\u0103<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p><strong>Cariotipul din s\u00e2nge fetal (cordon ombilical)<\/strong> este o analiz\u0103 citogenetic\u0103 clasic\u0103 bazat\u0103 pe <strong>cultur\u0103 celular\u0103 \u0219i bandare cromozomial\u0103 (G-banding)<\/strong>, utilizat\u0103 pentru evaluarea complet\u0103 a cariotipului fetal. Testul permite identificarea anomaliilor numerice \u0219i structurale ale cromozomilor \u00een perioada prenatal\u0103, prin analiz\u0103 direct\u0103 a limfocitelor fetale din s\u00e2ngele recoltat din cordonul ombilical.<\/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-104970","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=\"Cariotipul din s\u00e2nge fetal (cordon ombilical) este o analiz\u0103 citogenetic\u0103 clasic\u0103 bazat\u0103 pe cultur\u0103 celular\u0103 \u0219i bandare cromozomial\u0103 (G-banding), utilizat\u0103 pentru evaluarea complet\u0103 a cariotipului fetal. Testul permite identificarea anomaliilor numerice \u0219i structurale ale cromozomilor \u00een perioada prenatal\u0103, prin analiz\u0103 direct\u0103 a limfocitelor fetale din s\u00e2ngele recoltat din cordonul ombilical.\" \/>\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\/cultura-si-analiza-cromozomilor-din-sange-fetal-cariotip-sange-cordon-ombilical\/\" \/>\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=\"Cultura si analiza cromozomilor din sange fetal (cariotip sange cordon ombilical) - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"Cariotipul din s\u00e2nge fetal (cordon ombilical) este o analiz\u0103 citogenetic\u0103 clasic\u0103 bazat\u0103 pe cultur\u0103 celular\u0103 \u0219i bandare cromozomial\u0103 (G-banding), utilizat\u0103 pentru evaluarea complet\u0103 a cariotipului fetal. Testul permite identificarea anomaliilor numerice \u0219i structurale ale cromozomilor \u00een perioada prenatal\u0103, prin analiz\u0103 direct\u0103 a limfocitelor fetale din s\u00e2ngele recoltat din cordonul ombilical.\" \/>\n\t\t<meta property=\"og:url\" content=\"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/cultura-si-analiza-cromozomilor-din-sange-fetal-cariotip-sange-cordon-ombilical\/\" \/>\n\t\t<meta property=\"article:published_time\" content=\"2026-06-12T18:25:46+00:00\" \/>\n\t\t<meta property=\"article:modified_time\" content=\"2026-06-30T12:58:35+00:00\" \/>\n\t\t<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n\t\t<meta name=\"twitter:title\" content=\"Cultura si analiza cromozomilor din sange fetal (cariotip sange cordon ombilical) - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta name=\"twitter:description\" content=\"Cariotipul din s\u00e2nge fetal (cordon ombilical) este o analiz\u0103 citogenetic\u0103 clasic\u0103 bazat\u0103 pe cultur\u0103 celular\u0103 \u0219i bandare cromozomial\u0103 (G-banding), utilizat\u0103 pentru evaluarea complet\u0103 a cariotipului fetal. 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