{"id":27316,"date":"2025-06-24T14:54:33","date_gmt":"2025-06-24T12:54:33","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/cultura-si-analiza-cromozomilor-din-celulele-sangelui-periferic-cariotip-high-resolution\/"},"modified":"2026-02-27T18:00:48","modified_gmt":"2026-02-27T16:00:48","slug":"cultura-si-analiza-cromozomilor-din-celulele-sangelui-periferic-cariotip-high-resolution","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/cultura-si-analiza-cromozomilor-din-celulele-sangelui-periferic-cariotip-high-resolution\/","title":{"rendered":"Cultura si analiza cromozomilor din celulele sangelui periferic (CARIOTIP &#8211; High Resolution)"},"content":{"rendered":"<p>Cariotipul reprezint\u0103 <strong>imaginea complet\u0103 a setului de cromozomi ai unei persoane<\/strong>, ob\u021binut\u0103 prin tehnici citogenetice. \u00cen mod normal, fiecare celul\u0103 uman\u0103 con\u021bine <strong>46 de cromozomi (23 de perechi)<\/strong>.<\/p>\n<\/p>\n<p>Un set de 23 cromozomi este mo\u0219tenit de la mam\u0103 prin ovocit \u0219i unul de la tat\u0103 prin celula spermatic\u0103:<\/p>\n<\/p>\n<ul>\n<li>22 de perechi de <strong>cromozomi autozomi;<\/strong><\/li>\n<li>1 pereche de <strong>cromozomi sexuali<\/strong> (XX la femei, XY la b\u0103rba\u021bi).<\/li>\n<\/ul>\n<p>Analiza cariotipului presupune recoltarea de s\u00e2nge venos periferic, care este prelucrat \u00een laborator prin tehnici specifice de citogenetic\u0103, apoi cromozomii sunt ordona\u021bi dup\u0103 form\u0103 \u0219i dimensiune \u00een perechi, pentru a fi analiza\u021bi.<\/p>\n<\/p>\n<p>Analiza cromozomilor astfel ordona\u021bi poate identifica:<\/p>\n<\/p>\n<p>1. <strong>Anomalii numerice ale cromozomilor (aneuploidii)<\/strong> &#8211; prezen\u021ba unui cromozom suplimentar (trisomie) sau lipsa unui cromozom (monosomie).<\/p>\n<\/p>\n<ul>\n<li><strong>Exemple:<\/strong><\/li>\n<\/ul>\n<ul>\n<li>\n<ul>\n<li><strong>Trisomia 21 (sindrom Down)<\/strong><\/li>\n<li><strong>Monosomia X (sindrom Turner)<\/strong><\/li>\n<li><strong>47,XXY (sindrom Klinefelter)<\/strong><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>2. <strong>Anomalii structurale ale cromozomilor<\/strong><\/p>\n<\/p>\n<ul>\n<li><strong>Transloca\u021bii<\/strong> \u2013 schimb de material genetic \u00eentre cromozomi diferi\u021bi (reciproc\u0103 sau robertsonian\u0103). Pot fi echilibrate (f\u0103r\u0103 efect clinic direct) sau dezechilibrate (asociate cu pierdere\/exces de material genetic).<\/li>\n<li><strong>Dele\u021bii<\/strong> \u2013 pierderea unei por\u021biuni de cromozom.<\/li>\n<li><strong>Duplica\u021bii<\/strong> \u2013 dublarea unei por\u021biuni de cromozom.<\/li>\n<li><strong>Inversii<\/strong> \u2013 o secven\u021b\u0103 cromozomial\u0103 se rupe \u0219i se reintegreaz\u0103 inversat\u0103.<\/li>\n<li><strong>Inser\u021bii<\/strong> \u2013 o secven\u021b\u0103 dintr-un cromozom este introdus\u0103 \u00een altul.<\/li>\n<\/ul>\n<p>3. <strong>Rearanjamente cromozomiale complexe<\/strong><\/p>\n<\/p>\n<ul>\n<li>Asociate cu infertilitate, avorturi spontane recurente, boli hematologice sau risc de transmitere la descenden\u021bi.<\/li>\n<\/ul>\n<p class=\"ql-align-justify\"><strong>Metodologie de testare<\/strong><\/p>\n<p class=\"ql-align-justify\">\n<p class=\"ql-align-justify\">\u00a0Aceast\u0103 analiz\u0103 se realizeaz\u0103 printr-o tehnic\u0103 de <strong>citogenetic\u0103 clasic\u0103<\/strong>, ce presupune:<\/p>\n<p class=\"ql-align-justify\">\n<ul>\n<li>recoltarea de s\u00e2nge periferic;<\/li>\n<li>izolarea limfocitelor \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 class=\"ql-align-justify\">\u00cen cazul <strong>cariotipului High Resolution<\/strong>, analiza se face pe cromozomi afla\u021bi \u00eentr-un stadiu mai pu\u021bin condensat (prometafaz\u0103), ceea ce permite vizualizarea unui num\u0103r mai mare de benzi \u0219i detectarea unor modific\u0103ri mai mici dec\u00e2t la cariotipul standard.<\/p>\n<p class=\"ql-align-justify\">\n<p class=\"ql-align-justify\"><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<p class=\"ql-align-justify\">\n<p class=\"ql-align-justify\"><strong style=\"color: #ff9900\">C\u00e2nd este recomandat\u0103 analiza cromozomial\u0103 (cariotipul):<\/strong><\/p>\n<p class=\"ql-align-justify\">\n<ul>\n<li>La pacien\u021bi care au <strong>mai multe malforma\u021bii congenitale<\/strong>.<\/li>\n<li>La copii sau adul\u021bi cu <strong>\u00eent\u00e2rziere \u00een dezvoltare<\/strong> \u0219i <strong>tr\u0103s\u0103turi faciale neobi\u0219nuite<\/strong>.<\/li>\n<li>\u00cen cazul unor <strong>probleme de pubertate<\/strong>: menstrua\u021bie \u00eent\u00e2rziat\u0103 sau absent\u0103, caractere sexuale secundare slab dezvoltate.<\/li>\n<li>La pacien\u021bi cu <strong>ambiguitate sexual\u0103 la na\u0219tere<\/strong>.<\/li>\n<li>La persoane cu <strong>retard mintal de cauz\u0103 necunoscut\u0103<\/strong>, mai ales dac\u0103 au \u0219i tr\u0103s\u0103turi faciale anormale.<\/li>\n<li>La <strong>cupluri cu probleme de fertilitate<\/strong> sau cu <strong>avorturi repetate<\/strong>.<\/li>\n<li>La <strong>familiile<\/strong> \u00een care exist\u0103 deja un membru cu o anomalie cromozomial\u0103 cunoscut\u0103.<\/li>\n<\/ul>\n<p class=\"ql-align-justify\"><strong style=\"color: #ff9900\">C\u00e2nd NU se recomand\u0103 analiza cromozomial\u0103 (cariotipul):<\/strong><\/p>\n<p class=\"ql-align-justify\">\n<ul>\n<li>Dac\u0103 se suspecteaz\u0103 o <strong>afec\u021biune genetic\u0103 submicroscopic\u0103<\/strong> \u2192 se recomand\u0103 <strong>array-CGH (microarray)<\/strong>.<\/li>\n<li>Dac\u0103 se suspecteaz\u0103 o <strong>boal\u0103 cauzat\u0103 de o singur\u0103 gen\u0103<\/strong> \u2192 se recomand\u0103 <strong>secven\u021biere genetic\u0103<\/strong>.<\/li>\n<li>Dac\u0103 se suspecteaz\u0103 o <strong>boal\u0103 mitocondrial\u0103<\/strong> \u2192 se analizeaz\u0103 <strong>ADN-ul mitocondrial<\/strong>.<\/li>\n<li>Pentru <strong>boli multifactoriale<\/strong> (de exemplu: diabet, hipertensiune, boli cardiovasculare), \u00een care cauza nu este cromozomial\u0103.<\/li>\n<li>La <strong>cupluri \u00eenrudite (consangvine)<\/strong>, dac\u0103 nu au \u0219i alte indica\u021bii; \u00een aceste cazuri este mai util <strong>Carrier Screening<\/strong> (test care arat\u0103 riscul de boli genetice recesive la urma\u0219i).<\/li>\n<\/ul>\n<p class=\"ql-align-justify\"><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<p class=\"ql-align-justify\">\n<ul>\n<li>Analiza cromozomial\u0103 depisteaz\u0103 anomalii mari (cromozomi \u00een plus sau lips\u0103 ori rearanj\u0103ri vizibile).<\/li>\n<li>Pentru probleme mai fine (muta\u021bii mici, boli monogenice sau mitocondriale) sunt necesare teste genetice avansate.<\/li>\n<\/ul>\n<p class=\"ql-align-justify\">\n<p><strong>Recoltare \u0219i condi\u021bii:<\/strong><\/p>\n<\/p>\n<ul>\n<li>S\u00e2nge total recoltat pe heparin\u0103 sodic\u0103<\/li>\n<li>Proba poate fi recoltat\u0103 \u00een orice moment al zilei<\/li>\n<li>Nu este necesar postul alimentar \u00eenainte de recoltare<\/li>\n<li>Nu se recomand\u0103 efectuarea recolt\u0103rii \u00een timpul unei infec\u021bii acute (febr\u0103, infec\u021bii virale sau bacteriene)<\/li>\n<li>Se recomand\u0103 recoltarea la un interval de minimum 2 s\u0103pt\u0103m\u00e2ni de la vaccinare<\/li>\n<li>Se recomand\u0103 evitarea pe c\u00e2t posibil a tratamentelor care pot afecta diviziunea celular\u0103, \u00een special:\n<ul>\n<li>citostatice, imunosupresoare, radioterapie (pot inhiba proliferarea limfocitelor);<\/li>\n<li>antibiotice in doze mari,corticosteroizi,antivirale \u2013 pot influenta calitatea culturii.<\/li>\n<\/ul>\n<\/li>\n<li>\u00cen cazul unei transfuzii de s\u00e2nge se recomand\u0103 un interval de 4\u20138 s\u0103pt\u0103m\u00e2ni p\u00e2n\u0103 la recoltare.<\/li>\n<\/ul>\n<p><span style=\"color: black\">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<\/span><strong style=\"color: black\"> GRATUIT<\/strong><span style=\"color: black\"> \u0219i este destinat interpret\u0103rii rezultatelor \u0219i stabilirii indica\u021biilor terapeutice.<\/span><\/p>\n<\/p>\n<p><strong>E-mail: <\/strong><strong style=\"color: #ff9900\"><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 class=\"ql-align-justify\"><strong>Call Center:<\/strong> *8787<\/p>\n<p class=\"ql-align-justify\">\n<p class=\"ql-align-justify\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Aceast\u0103 investiga\u021bie reprezint\u0103 o metod\u0103 citogenetic\u0103 avansat\u0103 prin care se analizeaz\u0103 structura \u0219i num\u0103rul cromozomilor din celulele ob\u021binute din s\u00e2ngele periferic.<\/p>\n<\/p>\n<p>Genomul uman este format din molecule de ADN \u0219i este organizat sub forma a 23 de perechi de cromozomi (22 de perechi de autozomi \u0219i o pereche de gonozomi). <\/p>\n<\/p>\n<p>Pentru femei, un rezultat normal este 46,XX, iar pentru b\u0103rba\u021bi, un rezultat normal este 46,XY.<\/p>\n<\/p>\n<p>Comparativ cu cariotiparea clasic\u0103, tehnica HR (High Resolution) utilizeaz\u0103 un num\u0103r mai mare de benzi cromozomiale, ceea ce permite identificarea unor modific\u0103ri subtile \u0219i o interpretare mai detaliat\u0103 a genomului la nivel citogenetic.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3167,2876],"product_tag":[],"class_list":["post-27316","product","type-product","status-publish","product_cat-analize","product_cat-fertilitate-infertilitate-fiv","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=\"Aceast\u0103 investiga\u021bie reprezint\u0103 o metod\u0103 citogenetic\u0103 avansat\u0103 prin care se analizeaz\u0103 structura \u0219i num\u0103rul cromozomilor din celulele ob\u021binute din s\u00e2ngele periferic.Genomul uman este format din molecule de ADN \u0219i este organizat sub forma a 23 de perechi de cromozomi (22 de perechi de autozomi \u0219i o pereche de gonozomi). Pentru femei, un rezultat normal este 46,XX, iar pentru b\u0103rba\u021bi, un rezultat normal este 46,XY.Comparativ cu cariotiparea clasic\u0103, tehnica HR (High Resolution) utilizeaz\u0103 un num\u0103r mai mare de benzi cromozomiale, ceea ce permite identificarea unor modific\u0103ri subtile \u0219i o interpretare mai detaliat\u0103 a genomului la nivel citogenetic.\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<link rel=\"canonical\" href=\"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/cultura-si-analiza-cromozomilor-din-celulele-sangelui-periferic-cariotip-high-resolution\/\" \/>\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 celulele sangelui periferic (CARIOTIP \u2013 High Resolution) - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"Aceast\u0103 investiga\u021bie reprezint\u0103 o metod\u0103 citogenetic\u0103 avansat\u0103 prin care se analizeaz\u0103 structura \u0219i num\u0103rul cromozomilor din celulele ob\u021binute din s\u00e2ngele periferic.Genomul uman este format din molecule de ADN \u0219i este organizat sub forma a 23 de perechi de cromozomi (22 de perechi de autozomi \u0219i o pereche de gonozomi). Pentru femei, un rezultat normal este 46,XX, iar pentru b\u0103rba\u021bi, un rezultat normal este 46,XY.Comparativ cu cariotiparea clasic\u0103, tehnica HR (High Resolution) utilizeaz\u0103 un num\u0103r mai mare de benzi cromozomiale, ceea ce permite identificarea unor modific\u0103ri subtile \u0219i o interpretare mai detaliat\u0103 a genomului la nivel citogenetic.\" \/>\n\t\t<meta property=\"og:url\" content=\"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/cultura-si-analiza-cromozomilor-din-celulele-sangelui-periferic-cariotip-high-resolution\/\" \/>\n\t\t<meta property=\"article:published_time\" content=\"2025-06-24T12:54:33+00:00\" \/>\n\t\t<meta property=\"article:modified_time\" content=\"2026-02-27T16:00:48+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 celulele sangelui periferic (CARIOTIP \u2013 High Resolution) - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta name=\"twitter:description\" content=\"Aceast\u0103 investiga\u021bie reprezint\u0103 o metod\u0103 citogenetic\u0103 avansat\u0103 prin care se analizeaz\u0103 structura \u0219i num\u0103rul cromozomilor din celulele ob\u021binute din s\u00e2ngele periferic.Genomul uman este format din molecule de ADN \u0219i este organizat sub forma a 23 de perechi de cromozomi (22 de perechi de autozomi \u0219i o pereche de gonozomi). 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Pentru femei, un rezultat normal este 46,XX, iar pentru b\u0103rba\u021bi, un rezultat normal este 46,XY.Comparativ cu cariotiparea clasic\u0103, tehnica HR (High Resolution) utilizeaz\u0103 un num\u0103r mai mare de benzi cromozomiale, ceea ce permite identificarea unor modific\u0103ri subtile \u0219i o interpretare mai detaliat\u0103 a genomului la nivel citogenetic."},"aioseo_meta_data":{"post_id":"27316","title":null,"description":null,"keywords":null,"keyphrases":null,"primary_term":null,"canonical_url":null,"og_title":null,"og_description":null,"og_object_type":"default","og_image_type":"default","og_image_url":null,"og_image_width":null,"og_image_height":null,"og_image_custom_url":null,"og_image_custom_fields":null,"og_video":null,"og_custom_url":null,"og_article_section":null,"og_article_tags":null,"twitter_use_og":false,"twitter_card":"default","twitter_image_type":"default","twitter_image_url":null,"twitter_image_custom_url":null,"twitter_image_custom_fields":null,"twitter_title":null,"twitter_description":null,"schema":{"blockGraphs":[],"customGraphs":[],"default":{"data":{"Article":[],"Course":[],"Dataset":[],"FAQPage":[],"Movie":[],"Person":[],"Product":[],"ProductReview":[],"Car":[],"Recipe":[],"Service":[],"SoftwareApplication":[],"WebPage":[]},"graphName":"","isEnabled":true},"graphs":[]},"schema_type":"default","schema_type_options":null,"pillar_content":false,"robots_default":true,"robots_noindex":false,"robots_noarchive":false,"robots_nosnippet":false,"robots_nofollow":false,"robots_noimageindex":false,"robots_noodp":false,"robots_notranslate":false,"robots_max_snippet":null,"robots_max_videopreview":null,"robots_max_imagepreview":"large","priority":null,"frequency":null,"local_seo":null,"seo_analyzer_scan_date":"2026-08-26 17:34:35","breadcrumb_settings":null,"limit_modified_date":false,"open_ai":null,"ai":null,"created":"2025-06-24 14:37:17","updated":"2026-08-26 17:34:35","focus_keyword":null,"additional_keywords":null,"truseo_locale":null},"aioseo_breadcrumb":"<div class=\"aioseo-breadcrumbs\"><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/www.clinica-sante.com\/ro\" title=\"Prima pagin\u0103\">Prima pagin\u0103<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/www.clinica-sante.com\/ro\/analize-medicale\/\" title=\"Analize Medicale\">Analize Medicale<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/www.clinica-sante.com\/ro\/analize\/\" title=\"Analize\">Analize<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/www.clinica-sante.com\/ro\/analize-serviciu-laborator\/\" title=\"Serviciu laborator\">Serviciu laborator<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/\" title=\"Fertilitate\/Infertilitate\/FIV\">Fertilitate\/Infertilitate\/FIV<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\tCultura si analiza cromozomilor din celulele sangelui periferic (CARIOTIP \u2013 High Resolution)\n<\/span><\/div>","aioseo_breadcrumb_json":[{"label":"Prima pagin\u0103","link":"https:\/\/www.clinica-sante.com\/ro"},{"label":"Analize Medicale","link":"https:\/\/www.clinica-sante.com\/ro\/analize-medicale\/"},{"label":"Analize","link":"https:\/\/www.clinica-sante.com\/ro\/analize\/"},{"label":"Serviciu laborator","link":"https:\/\/www.clinica-sante.com\/ro\/analize-serviciu-laborator\/"},{"label":"Fertilitate\/Infertilitate\/FIV","link":"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/"},{"label":"Cultura si analiza cromozomilor din celulele sangelui periferic (CARIOTIP &#8211; 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