{"id":27323,"date":"2025-06-24T15:54:54","date_gmt":"2025-06-24T12:54:54","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/mutatie-factor-xiii\/"},"modified":"2026-07-02T08:44:26","modified_gmt":"2026-07-02T05:44:26","slug":"mutatie-factor-xiii","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-serviciu-laborator\/mutatie-factor-xiii\/","title":{"rendered":"Mutatie factor XIII"},"content":{"rendered":"<p>Factorul XIII este o protein\u0103 esen\u021bial\u0103 \u00een etapa final\u0103 a cascadei de coagulare, av\u00e2nd rolul de stabilizare a cheagului de fibrin\u0103 format \u00een procesul de hemostaz\u0103.<\/p>\n<p>Muta\u021biile genei <strong>F13A1<\/strong> pot duce la deficit de Factor XIII, determin\u00e2nd formarea unor cheaguri instabile, susceptibile la liza precoce. Aceast\u0103 disfunc\u021bie se asociaz\u0103 cu s\u00e2nger\u0103ri spontane sau post-traumatice \u0219i cu complica\u021bii obstetricale, inclusiv pierderi recurente de sarcin\u0103.<\/p>\n<p>De\u0219i rar\u0103, aceast\u0103 muta\u021bie are importan\u021b\u0103 clinic\u0103 semnificativ\u0103 \u00een evaluarea pacien\u021bilor cu istoric de s\u00e2nger\u0103ri inexplicabile sau infertilitate de cauz\u0103 hematologic\u0103.<\/p>\n<h3>Afec\u021biuni sau simptome asociate:<\/h3>\n<ul>\n<li>Deficit congenital de Factor XIII;<\/li>\n<li>S\u00e2nger\u0103ri spontane sau post-traumatice;<\/li>\n<li>Vindecare defectuoas\u0103 a pl\u0103gilor;<\/li>\n<li>Hematoame recurente;<\/li>\n<li>Hemoragii intracraniene (\u00een forme severe);<\/li>\n<li>Pierderi recurente de sarcin\u0103;<\/li>\n<li>Infertilitate sau complica\u021bii de implantare embrionar\u0103;<\/li>\n<li>S\u00e2nger\u0103ri post-operatorii prelungite.<\/li>\n<\/ul>\n<h3>Cui se adreseaz\u0103:<\/h3>\n<p>Medicilor hematologi, geneticienilor, obstetricienilor-ginecologi, speciali\u0219tilor \u00een medicin\u0103 reproductiv\u0103 \u0219i altor speciali\u0219ti implica\u021bi \u00een evaluarea tulbur\u0103rilor de coagulare sau pierderilor de sarcin\u0103 recurente.<\/p>\n<h3>Metodologie de testare:<\/h3>\n<p>Analiza este realizat\u0103 prin tehnici de biologie molecular\u0103 (de tip Real-Time PCR sau metode echivalente de genotipare) pe ADN genomic extras din s\u00e2nge periferic.<\/p>\n<p>Testul identific\u0103 variante patogene sau asociate cu deficitul de Factor XIII, \u00een special muta\u021bii din gena <strong>F13A1<\/strong>, responsabile de formele congenitale ale bolii.<\/p>\n<h3>Beneficii \u0219i importan\u021b\u0103 clinic\u0103:<\/h3>\n<ul>\n<li>Permite identificarea unei cauze rare de tulburare de coagulare;<\/li>\n<li>Explic\u0103 episoadele de s\u00e2ngerare inexplicabil\u0103;<\/li>\n<li>Important \u00een evaluarea pierderilor recurente de sarcin\u0103;<\/li>\n<li>Sprijin\u0103 diagnosticul diferen\u021bial al trombofiliilor \u0219i coagulopatiilor;<\/li>\n<li>Contribuie la consilierea genetic\u0103 familial\u0103;<\/li>\n<li>Ajut\u0103 la managementul obstetrical personalizat.<\/li>\n<\/ul>\n<h3>Particularit\u0103\u021bi \u0219i limit\u0103ri:<\/h3>\n<ul>\n<li>Este o analiz\u0103 pentru o afec\u021biune rar\u0103, cu prevalen\u021b\u0103 sc\u0103zut\u0103;<\/li>\n<li>Nu \u00eenlocuie\u0219te testele func\u021bionale ale Factorului XIII;<\/li>\n<li>Alte tulbur\u0103ri de coagulare pot coexista \u0219i trebuie investigate separat;<\/li>\n<li>Interpretarea trebuie corelat\u0103 cu tabloul clinic \u0219i testele de hemostaz\u0103.<\/li>\n<\/ul>\n<h3>Tip prob\u0103:<\/h3>\n<p>S\u00e2nge periferic (EDTA) \u2013 2 \u00d7 6 ml.<\/p>\n<h3>Recoltare:<\/h3>\n<p>Proba se recolteaz\u0103 \u00een vacutainer cu EDTA, conform standardelor pentru analize genetice.<\/p>\n<h3>Condi\u021bii:<\/h3>\n<p>Transport la 2\u20138\u00b0C.<\/p>\n<h3>Denumiri alternative:<\/h3>\n<ul>\n<li>Factor XIII muta\u021bie;<\/li>\n<li>F13A1 analiz\u0103 genetic\u0103;<\/li>\n<li>Deficit congenital Factor XIII;<\/li>\n<li>Test genetic coagulare Factor XIII;<\/li>\n<li>Trombofilie rar\u0103 Factor XIII;<\/li>\n<li>Analiz\u0103 molecular\u0103 hemostaz\u0103 final\u0103.<\/li>\n<\/ul>\n<h3>Analize asociate recomandate:<\/h3>\n<ul>\n<li>Activitatea Factor XIII plasmatic;<\/li>\n<li>Panel trombofilie ereditar\u0103 (F5, F2, MTHFR, PAI-1);<\/li>\n<li>Proteina C \u0219i Proteina S;<\/li>\n<li>Antitrombina III;<\/li>\n<li>Anticorpi antifosfolipidici;<\/li>\n<li>Evaluare hematologic\u0103 complet\u0103;<\/li>\n<li>Consiliere genetic\u0103.<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Analiz\u0103 genetic\u0103 molecular\u0103 utilizat\u0103 pentru detectarea muta\u021biilor din gena <strong>F13A1<\/strong>, asociate deficitului de Factor XIII, o cauz\u0103 rar\u0103 de tulbur\u0103ri de coagulare \u0219i complica\u021bii hemoragice, inclusiv s\u00e2nger\u0103ri recurente \u0219i pierderi de sarcin\u0103.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,2876,3215],"product_tag":[],"class_list":["post-27323","product","type-product","status-publish","product_cat-analize","product_cat-serviciu-laborator","product_cat-trombofilie","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 molecular\u0103 utilizat\u0103 pentru detectarea muta\u021biilor din gena F13A1, asociate deficitului de Factor XIII, o cauz\u0103 rar\u0103 de tulbur\u0103ri de coagulare \u0219i complica\u021bii hemoragice, inclusiv s\u00e2nger\u0103ri recurente \u0219i pierderi de sarcin\u0103.\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<link rel=\"canonical\" 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