{"id":26621,"date":"2025-06-24T14:12:47","date_gmt":"2025-06-24T12:12:47","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/panel-ngs-infertilitate-209-gene-ce-evalueaza-sarcini-pierdute-recurent-si-oprire-in-dezvoltarea-embrionara\/"},"modified":"2026-02-27T17:51:40","modified_gmt":"2026-02-27T15:51:40","slug":"panel-ngs-infertilitate-209-gene-ce-evalueaza-sarcini-pierdute-recurent-si-oprire-in-dezvoltarea-embrionara","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/panel-ngs-infertilitate-209-gene-ce-evalueaza-sarcini-pierdute-recurent-si-oprire-in-dezvoltarea-embrionara\/","title":{"rendered":"Panel NGS Infertilitate &gt;209 gene ce evalueaza sarcini pierdute recurent si oprire in dezvoltarea embrionara"},"content":{"rendered":"<p>Acest panel NGS ofer\u0103 o analiz\u0103 complet\u0103 a cauzelor genetice ale infertilit\u0103\u021bii, incluz\u00e2nd:<\/p>\n<\/p>\n<ul>\n<li>sarcini pierdute recurent la femei<\/li>\n<li>oprirea dezvolt\u0103rii embrionare<\/li>\n<li>factor masculin: afectarea spermatogenezei, motilit\u0103\u021bii spermei, structura spermatozoizilor<\/li>\n<li>factor feminin: disfunc\u021bii ovariene, insuficien\u021b\u0103 ovarian\u0103 primar\u0103, defecte endometriale<\/li>\n<\/ul>\n<p> Analiza ambilor parteneri permite evaluarea compatibilit\u0103\u021bii genetice, detect\u00e2nd variabilele care pot conduce la pierderi recurente de sarcin\u0103 sau infertilitate de cuplu.<\/p>\n<\/p>\n<p><strong>Afec\u021biuni sau simptome asociate<\/strong><\/p>\n<\/p>\n<ul>\n<li>infertilitate primar\u0103 sau secundar\u0103<\/li>\n<li>sarcini pierdute repetat (recurente)<\/li>\n<li>oprire \u00een dezvoltarea embrionar\u0103 sau avort spontan<\/li>\n<li>dezechilibre hormonale reproductive<\/li>\n<li>deficien\u021be gametice la b\u0103rba\u021bi sau femei<\/li>\n<li>sindroame genetice asociate cu infertilitate<\/li>\n<\/ul>\n<p><strong>Cui se adreseaz\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>cuplurilor care \u00eencearc\u0103 concep\u021bia f\u0103r\u0103 succes<\/li>\n<li>persoanelor cu istoric familial de pierderi recurente de sarcin\u0103<\/li>\n<li>femeilor cu avorturi spontane repetate<\/li>\n<li>b\u0103rba\u021bilor cu factor seminal anormal<\/li>\n<li>clinicienilor din medicin\u0103 reproductiv\u0103 \u0219i genetic\u0103<\/li>\n<\/ul>\n<p><strong>Metodologie de testare<\/strong><\/p>\n<\/p>\n<ul>\n<li>secven\u021biere NGS a exonilor \u0219i regiunilor critice<\/li>\n<li>detecteaz\u0103 variante punctiforme, inser\u021bii \u0219i dele\u021bii<\/li>\n<\/ul>\n<p><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>identific\u0103 cauze genetice ale infertilit\u0103\u021bii \u0219i pierderilor recurente de sarcin\u0103<\/li>\n<li>permite planificarea optim\u0103 a tratamentului reproductiv<\/li>\n<li>ofer\u0103 informa\u021bii pentru consiliere genetic\u0103 a cuplului<\/li>\n<li>ajut\u0103 la preven\u021bia transmiterii muta\u021biilor c\u0103tre descenden\u021bi<\/li>\n<li>sprijin\u0103 selec\u021bia strategic\u0103 a tehnicilor de reproducere asistat\u0103<\/li>\n<\/ul>\n<p><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<\/p>\n<ul>\n<li><strong>n<\/strong>u detecteaz\u0103 cauzele non-genetice de infertilitate (ex. hormonale, anatomice, infec\u021bioase)<\/li>\n<li>varianta de semnifica\u021bie incert\u0103 (VUS) necesit\u0103 corelare clinic\u0103<\/li>\n<li>nu exclude influen\u021ba factorilor de mediu sau a stilului de via\u021b\u0103<\/li>\n<\/ul>\n<p><strong>Recoltare \u0219i condi\u021bii<\/strong><\/p>\n<\/p>\n<ul>\n<li>probele se recolteaz\u0103 \u00een vacutainer cu EDTA<\/li>\n<li>nu sunt necesare condi\u021bii speciale de post<\/li>\n<\/ul>\n<p><strong>Analize asociate recomandate<\/strong><\/p>\n<\/p>\n<ul>\n<li>evaluare hormonal\u0103 (FSH, LH, AMH, prolactin\u0103, testosteron)<\/li>\n<li>analize spermogram\u0103 \u0219i test de fragmentare ADN spermatic<\/li>\n<li>teste genetice suplimentare pentru cuplu \u00een caz de sindroame asociate<\/li>\n<li>consiliere genetic\u0103 pre- \u0219i post-test<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Panelul analizeaz\u0103 209 gene asociate cu infertilitate masculin\u0103 \u0219i feminin\u0103, pierderi recurente de sarcin\u0103 \u0219i oprirea dezvolt\u0103rii embrionare.<\/p>\n<p> Testul poate fi efectuat simultan pentru ambii parteneri, oferind o evaluare genetic\u0103 complet\u0103 a cauzelor reproductive.<\/p>\n<p><strong>Gene analizate:<\/strong><\/p>\n<p> AIP, AIRE, AMH, AMHR2, ANOS1, ANXA5, BMP15, BMP4, BTG4, BTK, C1QC, C4BPA, CAPN10, CATSPER1, CASR, CD46, CDC73, CEP250, CDH23, CGB3, CHD7, CLPP, CYP11A1, CYP17A1, CYP19A1, CYP21A2, CNOT6L, CTNNA3, CPE, DIO1, DYNC2H1, DIAPH2, DMC1, DNAH1, DNAH5, DUOX2, DUOXA2, DUSP6, DPY19L2, EED, EIF2B2, EIF2B4, EIF2B5, ESR1, ESR2, ERCC6, F2, FANCM, FBXO43, FEZF1, FGF17, FGF8, FGFR1, FIGLA, FLRT3, FMR1, FOXE1, FOXL2, FOXP3, FSHB, FSHR, GALNT15, GALT, GATA3, GCM2, GDF9, GGPS1, GH1, GHR, GHRHR, GLE1, GLIS3, GNA11, GNAS, GNRH1, GNRHR, GPR101, HAMP, HARS2, HESX1, HFE, HFM1, HLA-G, HS6ST1, HSD17B4, HSD3B2, HSF2BP, IGSF1, IGSF10, IL17RD, ITGB3, IRS1, IRS4, IYD, KCNH2, KCNQ1, KHDC3L, KLHL10, KIF14, KISS1, KISS1R, LARS2, LAS1L, LHB, LHCGR, LHX3, LHX4, MCM8, MCM9, MECP2, MEI1, MTHFR, MOS, MSH4, MSH5, MRPS22, NLRP7, NANOG, NANOS1, NDNF, NKX2-1, NKX2-5, NLRP5, NLRP7, NLRP10, NOBOX, NUP107, NR0B1, NR5A1, NSMF, OTX2, OSBPL5, PADI6, PANX1, PATL2, PAX8, PICK1, PLCB2, PMM2, POF1B, POU1F1, POU5F1, PROK2, PROKR1, PROKR2, PROP1, PRORP, PSMC3IP, PTH, RNPC3, RYR1, SCN5A, SECISBP2, SEMA3A, SEPTIN12, SERPINE1, SYCP3, SLC16A2, SLC26A4, SLC26A8, SPATA16, SLC40A1, SLC5A5, SOHLH1, SOX10, SOX2, SOX3, SPIDR, SPP1, SPRY4, STAG3, STAT3, STK11, SUN5, SYCE1, TAC3, TACR3, TAF4B, TBCE, TBL1X, TCF12, TERT, TEX11, TEX15, TFR2, TG, THRA, THRB, TIMP2, TLE6, TPO, TRHR, TRIP13, TSHB, TSHR, TTF1, TUBB8, TWNK, UBR1, USP8, VSIG4, WDR11, WEE2, WNT6, ZFP42, ZP1, ZP2, ZP3, ZPBP.<\/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-26621","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=\"Panelul analizeaz\u0103 209 gene asociate cu infertilitate masculin\u0103 \u0219i feminin\u0103, pierderi recurente de sarcin\u0103 \u0219i oprirea dezvolt\u0103rii embrionare. Testul poate fi efectuat simultan pentru ambii parteneri, oferind o evaluare genetic\u0103 complet\u0103 a cauzelor reproductive.Gene analizate: AIP, AIRE, AMH, AMHR2, ANOS1, ANXA5, BMP15, BMP4, BTG4, BTK, C1QC, C4BPA, CAPN10, CATSPER1, CASR, CD46, CDC73, CEP250, CDH23, CGB3, CHD7, CLPP, CYP11A1, CYP17A1, CYP19A1, CYP21A2, CNOT6L, CTNNA3, CPE, DIO1, DYNC2H1, DIAPH2, DMC1, DNAH1, DNAH5, DUOX2, DUOXA2, DUSP6, DPY19L2, EED, EIF2B2, EIF2B4, EIF2B5, ESR1, ESR2, ERCC6, F2, FANCM, FBXO43, FEZF1, FGF17, FGF8, FGFR1, FIGLA, FLRT3, FMR1, FOXE1, FOXL2, FOXP3, FSHB, FSHR, GALNT15, GALT, GATA3, GCM2, GDF9, GGPS1, GH1, GHR, GHRHR, GLE1, GLIS3, GNA11, GNAS, GNRH1, GNRHR, GPR101, HAMP, HARS2, HESX1, HFE, HFM1, HLA-G, HS6ST1, HSD17B4, HSD3B2, HSF2BP, IGSF1, IGSF10, IL17RD, ITGB3, IRS1, IRS4, IYD, KCNH2, KCNQ1, KHDC3L, KLHL10, KIF14, KISS1, KISS1R, LARS2, LAS1L, LHB, LHCGR, LHX3, LHX4, MCM8, MCM9, MECP2, MEI1, MTHFR, MOS, MSH4, MSH5, MRPS22, NLRP7, NANOG, NANOS1, NDNF, NKX2-1, NKX2-5, NLRP5, NLRP7, NLRP10, NOBOX, NUP107, NR0B1, NR5A1, NSMF, OTX2, OSBPL5, PADI6, PANX1, PATL2, PAX8, PICK1, PLCB2, PMM2, POF1B, POU1F1, POU5F1, PROK2, PROKR1, PROKR2, PROP1, PRORP, PSMC3IP, PTH, RNPC3, RYR1, SCN5A, SECISBP2, SEMA3A, SEPTIN12, SERPINE1, SYCP3, SLC16A2, SLC26A4, SLC26A8, SPATA16, SLC40A1, SLC5A5, SOHLH1, SOX10, SOX2, SOX3, SPIDR, SPP1, SPRY4, STAG3, STAT3, STK11, SUN5, SYCE1, TAC3, TACR3, TAF4B, TBCE, TBL1X, TCF12, TERT, TEX11, TEX15, TFR2, TG, THRA, THRB, TIMP2, TLE6, TPO, TRHR, TRIP13, TSHB, TSHR, TTF1, TUBB8, TWNK, UBR1, USP8, VSIG4, WDR11, WEE2, WNT6, ZFP42, ZP1, ZP2, ZP3, ZPBP.\" \/>\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\/panel-ngs-infertilitate-209-gene-ce-evalueaza-sarcini-pierdute-recurent-si-oprire-in-dezvoltarea-embrionara\/\" \/>\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=\"Panel NGS Infertilitate &gt;209 gene ce evalueaza sarcini pierdute recurent si oprire in dezvoltarea embrionara - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"Panelul analizeaz\u0103 209 gene asociate cu infertilitate masculin\u0103 \u0219i feminin\u0103, pierderi recurente de sarcin\u0103 \u0219i oprirea dezvolt\u0103rii embrionare. Testul poate fi efectuat simultan pentru ambii parteneri, oferind o evaluare genetic\u0103 complet\u0103 a cauzelor reproductive.Gene analizate: AIP, AIRE, AMH, AMHR2, ANOS1, ANXA5, BMP15, BMP4, BTG4, BTK, C1QC, C4BPA, CAPN10, CATSPER1, CASR, CD46, CDC73, CEP250, CDH23, CGB3, CHD7, CLPP, CYP11A1, CYP17A1, CYP19A1, CYP21A2, CNOT6L, CTNNA3, CPE, DIO1, DYNC2H1, DIAPH2, DMC1, DNAH1, DNAH5, DUOX2, DUOXA2, DUSP6, DPY19L2, EED, EIF2B2, EIF2B4, EIF2B5, ESR1, ESR2, ERCC6, F2, FANCM, FBXO43, FEZF1, FGF17, FGF8, FGFR1, FIGLA, FLRT3, FMR1, FOXE1, FOXL2, FOXP3, FSHB, FSHR, GALNT15, GALT, GATA3, GCM2, GDF9, GGPS1, GH1, GHR, GHRHR, GLE1, GLIS3, GNA11, GNAS, GNRH1, GNRHR, GPR101, HAMP, HARS2, HESX1, HFE, HFM1, HLA-G, HS6ST1, HSD17B4, HSD3B2, HSF2BP, IGSF1, IGSF10, IL17RD, ITGB3, IRS1, IRS4, IYD, KCNH2, KCNQ1, KHDC3L, KLHL10, KIF14, KISS1, KISS1R, LARS2, LAS1L, LHB, LHCGR, LHX3, LHX4, MCM8, MCM9, MECP2, MEI1, MTHFR, MOS, MSH4, MSH5, MRPS22, NLRP7, NANOG, NANOS1, NDNF, NKX2-1, NKX2-5, NLRP5, NLRP7, NLRP10, NOBOX, NUP107, NR0B1, NR5A1, NSMF, OTX2, OSBPL5, PADI6, PANX1, PATL2, PAX8, PICK1, PLCB2, PMM2, POF1B, POU1F1, POU5F1, PROK2, PROKR1, PROKR2, PROP1, PRORP, PSMC3IP, PTH, RNPC3, RYR1, SCN5A, SECISBP2, SEMA3A, SEPTIN12, SERPINE1, SYCP3, SLC16A2, SLC26A4, SLC26A8, SPATA16, SLC40A1, SLC5A5, SOHLH1, SOX10, SOX2, SOX3, SPIDR, SPP1, SPRY4, STAG3, STAT3, STK11, SUN5, SYCE1, TAC3, TACR3, TAF4B, TBCE, TBL1X, TCF12, TERT, TEX11, TEX15, TFR2, TG, THRA, THRB, TIMP2, TLE6, TPO, TRHR, TRIP13, TSHB, TSHR, TTF1, TUBB8, TWNK, UBR1, USP8, VSIG4, WDR11, WEE2, WNT6, ZFP42, ZP1, ZP2, ZP3, ZPBP.\" \/>\n\t\t<meta property=\"og:url\" content=\"https:\/\/www.clinica-sante.com\/ro\/analize-fertilitate-infertilitate-fiv\/panel-ngs-infertilitate-209-gene-ce-evalueaza-sarcini-pierdute-recurent-si-oprire-in-dezvoltarea-embrionara\/\" \/>\n\t\t<meta property=\"article:published_time\" content=\"2025-06-24T12:12:47+00:00\" \/>\n\t\t<meta property=\"article:modified_time\" content=\"2026-02-27T15:51:40+00:00\" \/>\n\t\t<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n\t\t<meta name=\"twitter:title\" content=\"Panel NGS Infertilitate &gt;209 gene ce evalueaza sarcini pierdute recurent si oprire in dezvoltarea embrionara - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta name=\"twitter:description\" content=\"Panelul analizeaz\u0103 209 gene asociate cu infertilitate masculin\u0103 \u0219i feminin\u0103, pierderi recurente de sarcin\u0103 \u0219i oprirea dezvolt\u0103rii embrionare. Testul poate fi efectuat simultan pentru ambii parteneri, oferind o evaluare genetic\u0103 complet\u0103 a cauzelor reproductive.Gene analizate: AIP, AIRE, AMH, AMHR2, ANOS1, ANXA5, BMP15, BMP4, BTG4, BTK, C1QC, C4BPA, CAPN10, CATSPER1, CASR, CD46, CDC73, CEP250, CDH23, CGB3, CHD7, CLPP, CYP11A1, CYP17A1, CYP19A1, CYP21A2, CNOT6L, CTNNA3, CPE, DIO1, DYNC2H1, DIAPH2, DMC1, DNAH1, DNAH5, DUOX2, DUOXA2, DUSP6, DPY19L2, EED, EIF2B2, EIF2B4, EIF2B5, ESR1, ESR2, ERCC6, F2, FANCM, FBXO43, FEZF1, FGF17, FGF8, FGFR1, FIGLA, FLRT3, FMR1, FOXE1, FOXL2, FOXP3, FSHB, FSHR, GALNT15, GALT, GATA3, GCM2, GDF9, GGPS1, GH1, GHR, GHRHR, GLE1, GLIS3, GNA11, GNAS, GNRH1, GNRHR, GPR101, HAMP, HARS2, HESX1, HFE, HFM1, HLA-G, HS6ST1, HSD17B4, HSD3B2, HSF2BP, IGSF1, IGSF10, IL17RD, ITGB3, IRS1, IRS4, IYD, KCNH2, KCNQ1, KHDC3L, KLHL10, KIF14, KISS1, KISS1R, LARS2, LAS1L, LHB, LHCGR, LHX3, LHX4, MCM8, MCM9, MECP2, MEI1, MTHFR, MOS, MSH4, MSH5, MRPS22, NLRP7, NANOG, NANOS1, NDNF, NKX2-1, NKX2-5, NLRP5, NLRP7, NLRP10, NOBOX, NUP107, NR0B1, NR5A1, NSMF, OTX2, OSBPL5, PADI6, PANX1, PATL2, PAX8, PICK1, PLCB2, PMM2, POF1B, POU1F1, POU5F1, PROK2, PROKR1, PROKR2, PROP1, PRORP, PSMC3IP, PTH, RNPC3, RYR1, SCN5A, SECISBP2, SEMA3A, SEPTIN12, SERPINE1, SYCP3, SLC16A2, SLC26A4, SLC26A8, SPATA16, SLC40A1, SLC5A5, SOHLH1, SOX10, SOX2, SOX3, SPIDR, SPP1, SPRY4, STAG3, STAT3, STK11, SUN5, SYCE1, TAC3, TACR3, TAF4B, TBCE, TBL1X, TCF12, TERT, TEX11, TEX15, TFR2, TG, THRA, THRB, TIMP2, TLE6, TPO, TRHR, TRIP13, TSHB, TSHR, TTF1, TUBB8, TWNK, UBR1, USP8, VSIG4, WDR11, WEE2, WNT6, ZFP42, ZP1, ZP2, ZP3, ZPBP.\" \/>\n\t\t<script type=\"application\/ld+json\" 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