{"id":26663,"date":"2025-06-24T14:15:22","date_gmt":"2025-06-24T12:15:22","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/sangene-nipt-basic-sarcina-gemelara\/"},"modified":"2026-02-27T17:52:10","modified_gmt":"2026-02-27T15:52:10","slug":"sangene-nipt-basic-sarcina-gemelara","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-genetica-in-sarcina\/sangene-nipt-basic-sarcina-gemelara\/","title":{"rendered":"SanGene NIPT Basic (sarcina gemelara)"},"content":{"rendered":"<p class=\"ql-align-justify\"><strong>SanGene NIPT Basic<\/strong> (sarcin\u0103 unic\u0103 sau gemelar\u0103) este un test non-invaziv, care nu prezint\u0103 riscuri pentru mam\u0103 sau f\u0103t, fiind efectuat printr-o simpl\u0103 recoltare de s\u00e2nge matern. SanGene NIPT poate fi efectuat \u00eenc\u0103 din s\u0103pt\u0103m\u00e2na a 10-a de sarcin\u0103, oferind precoce informa\u021bii importante pentru managementul ulterior al sarcinii.<\/p>\n<p class=\"ql-align-justify\">\n<p class=\"ql-align-justify\">De\u0219i SanGene NIPT Basic (sarcin\u0103 unic\u0103 sau gemelar\u0103) nu este un test de diagnostic \u0219i rezultatele pozitive necesit\u0103 confirmarea prin teste de diagnostic din lichid amniotic sau din vilozit\u0103\u021bi coriale, acesta permite screeningul extins, cu acurate\u021be ridicat\u0103, pentru o serie extins\u0103 de afec\u021biuni genetice cu impact clinic.<\/p>\n<p class=\"ql-align-justify\">\n<p class=\"ql-align-justify\">Proba de s\u00e2nge poate fi recoltat\u0103 \u00een orice moment al zilei, f\u0103r\u0103 a fi necesar postul alimentar.<\/p>\n<p class=\"ql-align-justify\">\n<p>Societ\u0103\u021bi interna\u021bionale, precum Colegiul American al Obstetricienilor \u0219i Ginecologilor (ACOG), afirm\u0103 c\u0103 toate femeile \u00eens\u0103rcinate ar trebui s\u0103 fie informate despre op\u021biunile de screening NIPT pentru aneuploidii comune.<\/p>\n<\/p>\n<p><strong>Afec\u021biunile genetice incluse \u00een panelul de testare:<\/strong><\/p>\n<\/p>\n<p><strong style=\"color: #ff9900\">1. Aneuploidii comune<\/strong><\/p>\n<\/p>\n<p><strong>Trisomia 13 (Sindromul Patau)<\/strong><\/p>\n<\/p>\n<p><strong>Manifest\u0103ri clinice:<\/strong><\/p>\n<\/p>\n<ul>\n<li>retard mintal sever;<\/li>\n<li>microcefalie, holoprozencefalie (malforma\u021bii cerebrale);<\/li>\n<li>fante palatine \u0219i buz\u0103 despicat\u0103;<\/li>\n<li>polidactilie (degete suplimentare);<\/li>\n<li>malforma\u021bii cardiace \u0219i renale;<\/li>\n<li>supravie\u021buire redus\u0103 (majoritatea deceselor \u00een primul an).<\/li>\n<\/ul>\n<p><strong>Trisomia 18 (Sindromul Edwards)<\/strong><\/p>\n<\/p>\n<p><strong>Manifest\u0103ri clinice:<\/strong><\/p>\n<\/p>\n<ul>\n<li>retard mintal sever;<\/li>\n<li>cre\u0219tere intrauterin\u0103 \u00eent\u00e2rziat\u0103;<\/li>\n<li>craniu mic, occiput proeminent;<\/li>\n<li>urechi jos inserate, mandibul\u0103 mic\u0103;<\/li>\n<li>pozi\u021bie caracteristic\u0103 a m\u00e2inilor (pumn str\u00e2ns, degete suprapuse);<\/li>\n<li>malforma\u021bii cardiace \u0219i renale;<\/li>\n<li>speran\u021b\u0103 de via\u021b\u0103 foarte limitat\u0103.<\/li>\n<\/ul>\n<p><strong>Trisomia 21 (Sindromul Down)<\/strong><\/p>\n<\/p>\n<p><strong>Manifest\u0103ri clinice:<\/strong><\/p>\n<\/p>\n<ul>\n<li>retard mintal variabil;<\/li>\n<li>facies tipic: profil plat, epicantus, limb\u0103 mare;<\/li>\n<li>hipotonie neonatal\u0103;<\/li>\n<li>plis palmar unic;<\/li>\n<li>malforma\u021bii cardiace (defect septal atrioventricular frecvent);<\/li>\n<li>risc crescut de leucemii \u0219i boal\u0103 Alzheimer precoce.<\/li>\n<\/ul>\n<p><strong style=\"color: #ff9900\">2. Sexul fetal pentru sarcinile unice si detec\u021bia prezen\u021bei cromozomului Y pentru sarcinile gemelare<\/strong><\/p>\n<\/p>\n<p><strong>Cui se adreseaz\u0103 analiza:<\/strong><\/p>\n<\/p>\n<ul>\n<li>at\u00e2t sarcinilor cu un singur f\u0103t, c\u00e2t \u0219i sarcinilor gemelare;<\/li>\n<li>femeilor \u00eens\u0103rcinate de orice v\u00e2rst\u0103, \u00een special celor peste 35 de ani;<\/li>\n<li>cuplurilor cu antecedente de anomalii genetice \u00een familie;<\/li>\n<li>femeilor care au avut rezultate anormale la alte teste de screening prenatal (dublu\/triplu test, morfologie fetal\u0103 etc.);<\/li>\n<li>sarcinilor ob\u021binute prin FIV, inclusiv sarcinilor cu ovocite donate sau mam\u0103 surogat.<\/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\"><strong>SanGene NIPT<\/strong> utilizeaz\u0103 tehnologia NGS paired-end, secven\u021bierea \u00eentregului genom (whole genome sequencing), pentru analiza ADN-ului fetal liber circulant prezent \u00een s\u00e2ngele matern.<\/p>\n<\/p>\n<p class=\"ql-align-justify\"><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<p class=\"ql-align-justify\">\n<ul>\n<li>Secven\u021bierea de tip NGS paired-end permite diferen\u021bierea \u00eentre ADN-ul fetal liber circulant \u0219i ADN-ul matern, ceea ce \u00eembun\u0103t\u0103\u021be\u0219te evaluarea frac\u021biei fetale \u0219i cre\u0219te performan\u021bele testului.<\/li>\n<li>Spre deosebire de alte metode de testare NIPT, aceast\u0103 tehnic\u0103 furnizeaz\u0103 un volum mai mare de informa\u021bii \u00eentr-un timp mai scurt, fiind eliminate posibilele surse de eroare care pot ap\u0103rea \u00een cazul secven\u021bierii \u021bintite sau al microarray.<\/li>\n<li>Testul are specificitate \u0219i sensibilitate crescute (&gt;99%), ceea ce reduce num\u0103rul de rezultate fals pozitive, evit\u00e2nd astfel proceduri invazive inutile.<\/li>\n<li>Utilizeaz\u0103 tehnologia NGS pentru secven\u021bierea \u00eentregului genom fetal, ceea ce permite detectarea unei game largi de anomalii cromozomiale.<\/li>\n<\/ul>\n<p class=\"ql-align-justify\">\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>Testul poate fi efectuat at\u00e2t pentru sarcinile unice, c\u00e2t \u0219i pentru cele gemelare, ob\u021binute natural, dar \u0219i pentru sarcinile ob\u021binute prin FIV sau cu ovocite donate.<\/li>\n<li>Testul poate fi efectuat doar \u00eencep\u00e2nd cu s\u0103pt\u0103m\u00e2na a 10-a de sarcin\u0103.<\/li>\n<li>Testul nu poate fi efectuat pentru sarcinile cu mai mult de 2 fe\u021bi.<\/li>\n<li>Testul este destinat screeningului, iar rezultatele pozitive necesit\u0103 confirmare printr-un test de diagnostic.<\/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 \u00een recipient special: Vacutainer Streck 1 \u00d7 10 mL;<\/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>\u00een cazul unei transfuzii de s\u00e2nge se recomand\u0103 un interval de minim 4 s\u0103pt\u0103m\u00e2ni (ideal 8 s\u0103pt\u0103m\u00e2ni) \u00eenainte de recoltare.<\/li>\n<\/ul>\n<p><strong>Analize asociate recomandate:<\/strong><\/p>\n<\/p>\n<ul>\n<li>Screening status de purt\u0103tor \u2013 420 gene \u2013 Carrier Screening 420 genes \u2013 for patients<\/li>\n<li>Carrier Screening avansat bazat pe exom (cu analiza a 2.423 gene)<\/li>\n<li>Screening status de purt\u0103tor pentru muta\u021biile CFTR F508del (fibroza chistic\u0103) \u0219i GJB2 35delG (surditate genetic\u0103)<\/li>\n<li>Detec\u021bie muta\u021bie GJB2 35delG (surditate genetic\u0103)<\/li>\n<li>Detec\u021bie muta\u021bie F508del (fibroza chistic\u0103)<\/li>\n<li>dublu test (determinare parametri biochimici free \u03b2-hCG \u0219i PAPP-A, Kryptor)<\/li>\n<li>dublu test (screening prenatal trimestrul I, 11\u201313 s\u0103pt\u0103m\u00e2ni \u0219i 6 zile)<\/li>\n<li>DRY TEST trimestrul I de sarcin\u0103 (bitest PRISCA \u0219i screening genetic al gravidei pentru muta\u021biile CFTR F508del \u0219i GJB2 35delG)<\/li>\n<li>evaluare risc preeclampsie (PAPP-A\/PlGF) (11\u201313.6 s\u0103pt\u0103m\u00e2ni)<\/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. Acesta din urm\u0103 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 style=\"color: black\">E-mail:<\/strong><span style=\"color: black\"> <\/span><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 style=\"color: black\">Telefon:<\/strong><span style=\"color: black\"> 0773.975.894<\/span><\/p>\n<\/p>\n<p><strong style=\"color: black\">Program:<\/strong><span style=\"color: black\"> Luni\u2013Vineri<\/span><\/p>\n<\/p>\n<p><strong style=\"color: black\">Orele: <\/strong><span style=\"color: black\">8:00\u201316:30<\/span><\/p>\n<\/p>\n<p><strong style=\"color: black\">Call Center:<\/strong><span style=\"color: black\"> *8787<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p><strong>SanGene NIPT Basic<\/strong> (sarcin\u0103 unic\u0103 sau gemelar\u0103) este destinat screeningului prenatal non-invaziv care detecteaz\u0103 posibile anomalii genetice ale f\u0103tului, \u00eenc\u0103 din s\u0103pt\u0103m\u00e2na a 10-a de sarcin\u0103, prin analiza ADN-ului fetal liber circulant din s\u00e2ngele matern.<\/p>\n<\/p>\n<p><strong>\u00cen cadrul acestui panel se face screening pentru:<\/strong><\/p>\n<\/p>\n<ul>\n<li>aneuplodiile comune: trisomia 13 (sindromul Patau), trisomia 18 (sindromul Edwards) \u0219i trisomia 21 (sindromul Down).<\/li>\n<li>sexul fetal (detectarea prezen\u021bei cromozomului Y).<\/li>\n<\/ul>\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":{"0":"post-26663","1":"product","2":"type-product","3":"status-publish","5":"product_cat-analize","6":"product_cat-genetica-in-sarcina","7":"product_cat-serviciu-laborator","8":"pa_genetica-genetica-in-sarcina","10":"first","11":"instock","12":"sale","13":"virtual","14":"purchasable","15":"product-type-simple"},"acf":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/product\/26663","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/types\/product"}],"wp:attachment":[{"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/media?parent=26663"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/product_brand?post=26663"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/product_cat?post=26663"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/www.clinica-sante.com\/ro\/wp-json\/wp\/v2\/product_tag?post=26663"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}