{"id":2219,"date":"2023-08-01T14:41:06","date_gmt":"2023-08-01T14:41:06","guid":{"rendered":"https:\/\/genoks.com.tr\/?p=2219"},"modified":"2026-04-30T10:47:35","modified_gmt":"2026-04-30T10:47:35","slug":"qeyri-invaziv-prenatal-test-nedir","status":"publish","type":"post","link":"https:\/\/genoks.com.tr\/az\/qeyri-invaziv-prenatal-test-nedir\/","title":{"rendered":"Qeyri-\u0130nvaziv Prenatal Test N\u0259dir?"},"content":{"rendered":"<p>Qeyri-invaziv prenatal test (NIPT), ana namiz\u0259dl\u0259ri v\u0259 s\u0259hiyy\u0259 pe\u015f\u0259karlar\u0131 \u00fc\u00e7\u00fcn prenatal qullu\u011fun \u00f6n\u0259mli bir hiss\u0259sidir. Ana namiz\u0259dinin v\u0259 k\u00f6rp\u0259sinin sa\u011flaml\u0131\u011f\u0131n\u0131 izl\u0259m\u0259k v\u0259 potensial riskl\u0259ri qiym\u0259tl\u0259ndirm\u0259k \u00fc\u00e7\u00fcn istifad\u0259 olunan etibarl\u0131 bir \u00fcsuldur.<\/p>\n<h2><strong>\u0130nvaziv N\u0259dir?<\/strong><\/h2>\n<p>\u0130nvaziv, v\u00fccud toxumalar\u0131na v\u0259 ya orqanlar\u0131na xaricd\u0259n m\u00fcdaxil\u0259 t\u0259l\u0259b ed\u0259n bir proses v\u0259 ya testi ifad\u0259 edir. Bel\u0259 m\u00fcdaxil\u0259l\u0259r ad\u0259t\u0259n d\u0259rid\u0259 de\u015fik a\u00e7\u0131lmas\u0131 v\u0259 ya toxuma b\u00fct\u00f6vl\u00fcy\u00fcn\u00fcn pozulmas\u0131 il\u0259 h\u0259yata ke\u00e7irilir.<\/p>\n<h2><strong>Qeyri-\u0130nvaziv Prenatal Test (NIPT) N\u0259dir?<\/strong><\/h2>\n<p>Qeyri-invaziv prenatal test (NIPT), hamil\u0259lik d\u00f6vr\u00fcnd\u0259 istifad\u0259 edil\u0259n olduqca \u00f6n\u0259mli v\u0259 effektiv bir genetik tarama \u00fcsuludur. K\u00f6rp\u0259l\u0259rin sa\u011flaml\u0131\u011f\u0131n\u0131 izl\u0259m\u0259k v\u0259 xromosom poz\u011funluqlar\u0131n\u0131 a\u015fkarlamaq \u00fc\u00e7\u00fcn ana qan\u0131ndan g\u00f6t\u00fcr\u00fcl\u0259n n\u00fcmun\u0259 il\u0259 apar\u0131l\u0131r.<\/p>\n<h3><strong>Qeyri-\u0130nvaziv Prenatal Testin (NIPT) \u00dcst\u00fcnl\u00fckl\u0259ri N\u0259l\u0259rdir?<\/strong><\/h3>\n<p>Qeyri-invaziv prenatal test, invaziv m\u00fcdaxil\u0259 t\u0259l\u0259b etm\u0259diyi v\u0259 minimal risk da\u015f\u0131d\u0131\u011f\u0131 \u00fc\u00e7\u00fcn ana v\u0259 k\u00f6rp\u0259 \u00fc\u00e7\u00fcn etibarl\u0131 bir se\u00e7imdir.<\/p>\n<p><strong>Genetik X\u0259st\u0259likl\u0259rin Erk\u0259n T\u0259\u015fxisi<\/strong><\/p>\n<p>Qeyri-invaziv prenatal test, ana qan\u0131ndak\u0131 s\u0259rb\u0259st fetal DNT-ni t\u0259hlil ed\u0259r\u0259k k\u00f6rp\u0259l\u0259rin DNT-sini a\u015fkar edir. Bu say\u0259d\u0259 Daun sindromu, Edvards sindromu, Patau sindromu kimi ciddi genetik x\u0259st\u0259likl\u0259rin taranmas\u0131n\u0131 h\u0259yata ke\u00e7irir. Bunlar\u0131n yan\u0131nda cinsi xromosom anomaliyalar\u0131 da a\u015fkarlana bil\u0259r.<\/p>\n<p><strong>S\u00fcr\u0259tli N\u0259tic\u0259l\u0259r<\/strong><\/p>\n<p><em>NIPT-nin y\u00fcks\u0259k d\u0259qiqlik d\u0259r\u0259c\u0259si say\u0259sind\u0259 n\u0259tic\u0259l\u0259r ad\u0259t\u0259n 3 il\u0259 5 i\u015f g\u00fcn\u00fc \u0259rzind\u0259 \u0259ld\u0259 edilir. Laz\u0131m olduqda<\/em> <strong><em>t\u0259sdiq testl\u0259rin\u0259 m\u00fcraci\u0259t etm\u0259k \u00fc\u00e7\u00fcn vaxt qazand\u0131r\u0131r.<\/em><\/strong><\/p>\n<h2><strong>RapidNIPT N\u0259dir?<\/strong><\/h2>\n<p>RapidNIPT, genetik tarama \u00fcsullar\u0131ndan biri olan qeyri-invaziv prenatal testin (NIPT) x\u00fcsusi bir versiyas\u0131d\u0131r. K\u00f6rp\u0259l\u0259rin genetik sa\u011flaml\u0131\u011f\u0131n\u0131 izl\u0259m\u0259k v\u0259 xromosom poz\u011funluqlar\u0131n\u0131 qiym\u0259tl\u0259ndirm\u0259k m\u0259qs\u0259dil\u0259 ana qan\u0131ndan g\u00f6t\u00fcr\u00fcl\u0259n n\u00fcmun\u0259 il\u0259 apar\u0131l\u0131r.<\/p>\n<p>RapidNIPT, \u0259sas\u0131nda ana qan\u0131ndak\u0131 s\u0259rb\u0259st fetal DNT-ni t\u0259hlil ed\u0259r\u0259k k\u00f6rp\u0259l\u0259rin DNT-sini ara\u015fd\u0131r\u0131r. Daun sindromu (Trisomiya 21), Edvards sindromu (Trisomiya 18), Patau sindromu (Trisomiya 13) kimi xromosom poz\u011funluqlar\u0131n\u0131 skrininq edir.<\/p>\n<p>Test n\u0259tic\u0259l\u0259ri ad\u0259t\u0259n <strong>3 il\u0259 5 i\u015f g\u00fcn\u00fc \u0259rzind\u0259<\/strong> \u0259ld\u0259 edilir. RapidNIPT, 70 f\u0259rqli xromosom x\u0259st\u0259liyinin taranmas\u0131n\u0131 t\u0259min edir.<\/p>\n<h3><strong>RapidNIPTPlus N\u0259dir?<\/strong><\/h3>\n<p>RapidNIPTPlus, RapidNIPT-nin qiym\u0259tl\u0259ndirdiyi 70 f\u0259rqli xromosom x\u0259st\u0259liyinin yan\u0131nda nisb\u0259t\u0259n tez-tez rast g\u0259lin\u0259n DiGeorge sindromunu da a\u015fkar ed\u0259 bilir.<\/p>\n<p>RapidNIPT haqq\u0131nda \u0259trafl\u0131 m\u0259lumat almaq \u00fc\u00e7\u00fcn <a href=\"http:\/\/www.rapidnipt.com.tr\/\" target=\"_blank\" rel=\"noopener noreferrer\">www.rapidnipt.com.tr<\/a> \u00fcnvan\u0131na daxil ola v\u0259 ya <a href=\"https:\/\/genoks.com.tr\/sikca-sorulan-sorular\/\" target=\"_blank\" rel=\"noopener noreferrer\">RapidNIPT haqq\u0131nda tez-tez veril\u0259n suallar\u0131n cavablar\u0131na buradan<\/a> baxa bil\u0259rsiniz.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Qeyri-invaziv prenatal test (NIPT) ana qan n\u00fcmun\u0259sind\u0259n Daun, Edvards v\u0259 Patau sindromlar\u0131 kimi xromosom anomaliyalar\u0131n\u0131 skrininq edir; ana v\u0259 k\u00f6rp\u0259 \u00fc\u00e7\u00fcn risksizdir.<\/p>\n","protected":false},"author":1,"featured_media":1195,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"image","meta":{"footnotes":""},"categories":[145],"tags":[135,137,138],"class_list":["post-2219","post","type-post","status-publish","format-image","has-post-thumbnail","hentry","category-genel","tag-bebegin-cinsiyeti-nasil-ogrenilir","tag-hamilelikte-bebegin-cinsiyeti-ne-zaman-belli-olur","tag-hamilelikte-cinsiyet-tahmini-nasil-yapilir","post_format-post-format-image"],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"Qeyri-invaziv prenatal test (NIPT) ana qan n\u00fcmun\u0259sind\u0259n Daun, Edvards v\u0259 Patau sindromlar\u0131 kimi xromosom anomaliyalar\u0131n\u0131 skrininq edir; ana v\u0259 k\u00f6rp\u0259 \u00fc\u00e7\u00fcn 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