{"id":2417,"date":"2023-05-30T11:39:02","date_gmt":"2023-05-30T11:39:02","guid":{"rendered":"https:\/\/genoks.com.tr\/genoks-testi-kac-gunde-cikar-me\/"},"modified":"2026-04-30T18:22:28","modified_gmt":"2026-04-30T18:22:28","slug":"genoks-testi-kac-gunde-cikar-me","status":"publish","type":"post","link":"https:\/\/genoks.com.tr\/me\/genoks-testi-kac-gunde-cikar-me\/","title":{"rendered":"Koliko dana je potrebno da se dobije Genok test? Koliko je potrebno?"},"content":{"rendered":"<p>Patentirani NIPT test Genoksovog centra za procenu genetskih bolesti (Koliko je potrebno da se Genoks test objavi?) RapidNIPT se prijavljuje u roku od 3 radna dana<\/strong>. U nekim slu\u010dajevima, ovaj period se mo\u017ee produ\u017eiti do 5 radnih dana.<\/p>\n<h4>\u0160ta je RapidNIPT?<\/h4>\n<p>RapidNIPT je skrining test nove generacije koji otkriva 70 razli\u010ditih hromozomskih bolesti, koji se prou\u010dava epruvetom krvi trudnice od 10. nedelje trudno\u0107e, a koji je neinvazivan i ni na koji na\u010din ne \u0161teti zdravlju budu\u0107e majke i bebe. <i>RapidNIPT <a href=\"https:\/\/vvv.illumina.com\/\">Illumina<\/a> koristi VeriSek NIPT Solution v2 tehnologiju.<\/i><\/p>\n<p>RapidNIPT, koji je NIPT test Centra za procenu genetskih bolesti Genoks, se izvodi brzo i sa 99% ta\u010dnosti, zahvaljuju\u0107i radu u laboratorijama Genoks Ankara. Pored parametara RapidNIPT testa, on tako\u0111e izve\u0161tava o retkim numeri\u010dkim hromozomskim anomalijama i delecijama\/duplikacijama odre\u0111ene veli\u010dine koje su otkrivene kao rezultat sekvence i za koje se smatra da pripadaju fetusu.<\/p>\n<p>Deleciju karakteri\u0161e gubitak segmenta hromozoma, dok se dupliranje karakteri\u0161e pove\u0107anjem segmenta hromozoma. Veli\u010dina, lokacija delecije\/duplikacije i geni koje sadr\u017ei odre\u0111uju klini\u010dke karakteristike sindroma koji se mogu javiti.<\/p>\n<p>Mo\u017ee izazvati klini\u010dke karakteristike kao \u0161to su sindromi delecije\/duplikacije, ka\u0161njenja u rastu\/razvoju, kognitivni deficiti, problemi u pona\u0161anju, pote\u0161ko\u0107e u hranjenju, promene mi\u0161i\u0107nog tonusa, napadi, dismorfni nalazi i razne malformacije.<\/p>\n<p>\u00a0<\/p>\n<table>\n<tbody>\n<tr>\n<td width=\"50%\">\n<h4>Human Chromosomes<\/h4>\n<p align=\"justify\">Deleciju karakteri\u0161e gubitak segmenta hromozoma, dok se dupliranje karakteri\u0161e pove\u0107anjem segmenta hromozoma. Veli\u010dina, lokacija delecije\/duplikacije i geni koje sadr\u017ei odre\u0111uju klini\u010dke karakteristike sindroma koji se mogu javiti. Mo\u017ee izazvati klini\u010dke karakteristike kao \u0161to su sindromi delecije\/duplikacije, ka\u0161njenja u rastu\/razvoju, kognitivni deficiti, problemi u pona\u0161anju, pote\u0161ko\u0107e u hranjenju, promene mi\u0161i\u0107nog tonusa, napadi, dismorfni nalazi i razne malformacije.<\/p>\n<\/td>\n<td><img decoding=\"async\" class=\"\" src=\"https:\/\/genoks.com.tr\/wp-content\/uploads\/2022\/04\/kromozom-listesi.jpeg\" alt=\"\u0130nsan Kromozomlar\u0131\" width=\"100%\" \/><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>\u00a0<\/p>\n<h4 style=\"text-align: center;\">Za koje bolesti pregledava RapidNIPT? (*\u2265 7 Mb je za brisanja i dupliranja.)<\/h4>\n<p>\u00a0<\/p>\n<table>\n<tbody>\n<tr>\n<td width=\"50%\">\n<ul>\n<li style=\"text-align: left;\">11k11-k13.3 Sindrom dupliranja<\/li>\n<li style=\"text-align: left;\">12k14 sindrom brisanja<\/li>\n<li style=\"text-align: left;\">14k11-k22 sindrom brisanja<\/li>\n<li style=\"text-align: left;\">15k26 Sindrom prekomernog rasta<\/li>\n<li style=\"text-align: left;\">16p11.2-p12.2 Sindrom brisanja<\/li>\n<li style=\"text-align: left;\">16p11.2-p12.2 Sindrom dupliranja<\/li>\n<li style=\"text-align: left;\">17k21.31 Sindrom brisanja<\/li>\n<li style=\"text-align: left;\">17k21.31 Sindrom dupliranja<\/li>\n<li style=\"text-align: left;\">1p36 sindrom brisanja<\/li>\n<li style=\"text-align: left;\">1k41-k42 sindrom brisanja<\/li>\n<li style=\"text-align: left;\">Glassov sindrom (2k33.1)<\/li>\n<li style=\"text-align: left;\">5k21.1-k31.2 Sindrom brisanja<\/li>\n<li style=\"text-align: left;\">8p23.1 Sindrom brisanja<\/li>\n<li style=\"text-align: left;\">8p23.1 Sindrom dupliranja<\/li>\n<li style=\"text-align: left;\">Alfa talasemija, sindrom mentalne retardacije (16p13.3)<\/li>\n<li style=\"text-align: left;\">Sindrom neosetljivosti na androgene (Ksk12)<\/li>\n<li style=\"text-align: left;\">Angelmanov sindrom\/Prader-Villi sindrom (15k11-k13)<\/li>\n<li style=\"text-align: left;\">Aniridija II i VAGR sindrom (11p13)<\/li>\n<li style=\"text-align: left;\">Bannaian-Rilei-Ruvalcaba sindrom (BRRS) (10k23.31)<\/li>\n<li style=\"text-align: left;\">Branhiootorenalna displazija P. 1 \/ Melnick-Fraser S. (8k13.3)<\/li>\n<li style=\"text-align: left;\">Sindrom ma\u010djeg oka (22k11.21)<\/li>\n<li style=\"text-align: left;\">Sindrom brisanja hromozoma 10k (10k26)<\/li>\n<li style=\"text-align: left;\">Sindrom brisanja hromozoma 10k22.3-k23.31<\/li>\n<li style=\"text-align: left;\">Sindrom brisanja hromozoma 18p<\/li>\n<li style=\"text-align: left;\">Sindrom brisanja hromozoma 18k<\/li>\n<li style=\"text-align: left;\">Sindrom Kornelije de Lange (5p13.2)<\/li>\n<li style=\"text-align: left;\">Kaudenov sindrom (10k23.31)<\/li>\n<li style=\"text-align: left;\">Cri du Chat sindrom (5p15.2)<\/li>\n<li style=\"text-align: left;\">Dandi-Vokerov sindrom (3k22-k24)<\/li>\n<li style=\"text-align: left;\">Kongenitalna dijafragmatska kila (HCD\/DIH1) (15k26.1)<\/li>\n<li style=\"text-align: left;\">DiGeorge 2 sindrom (DGS2) &#8211; (10p14-p13)<\/li>\n<li style=\"text-align: left;\">DistalArthrogriposisTipe 2B (9p13.3;11p15.5;17p13.1)<\/li>\n<\/ul>\n<\/td>\n<td>\n<ul>\n<li style=\"text-align: left;\">Duchenneova mi\u0161i\u0107na distrofija;<\/li>\n<li style=\"text-align: left;\">Duchenne\/Becker mi\u0161i\u0107na distrofija (Ksp21.2-p21.1)<\/li>\n<li style=\"text-align: left;\">Diggve-Melchior-Clausen sindrom (18k21.1)<\/li>\n<li style=\"text-align: left;\">Feingoldov sindrom I (2p24.3)<\/li>\n<li style=\"text-align: left;\">Holoprosencefalija tip 1 (21k22.3)<\/li>\n<li style=\"text-align: left;\">Holoprosencefalija tip 4 (18p11.31)<\/li>\n<li style=\"text-align: left;\">Holoprosencefalija tip 6 (2k37.1-k37.3)<\/li>\n<li style=\"text-align: left;\">Jakobsenov sindrom (11k24-k25)<\/li>\n<li style=\"text-align: left;\">Langer-Giedionov sindrom (8k23.3-k24.11)<\/li>\n<li style=\"text-align: left;\">Leukodistrofija S. (11k14.2-k14.3)<\/li>\n<li style=\"text-align: left;\">Sa nedostatkom hormona rasta<\/li>\n<li style=\"text-align: left;\">Mentalna retardacija S. (Ksk26-k27)<\/li>\n<li style=\"text-align: left;\">Mikroftalmije sa linearnim defektima ko\u017ee (Ksp22.2)<\/li>\n<li style=\"text-align: left;\">Microphthalmia S. Tip 6 sa hipoplazijom hipofize<\/li>\n<li style=\"text-align: left;\">(14k22.2-k22.3)<\/li>\n<li style=\"text-align: left;\">Sindrom monozomije 9p (9p22.3-p23)<\/li>\n<li style=\"text-align: left;\">Orofacijalni digitalni sindrom (Ksp22.2)<\/li>\n<li style=\"text-align: left;\">Panhipopituitarizam povezan sa Ks (Ksk26-k27)<\/li>\n<li style=\"text-align: left;\">Potocki-Lupski Send. (17p11.2 sindrom duplikacije)<\/li>\n<li style=\"text-align: left;\">6k16.3 Brisanje<\/li>\n<li style=\"text-align: left;\">Rigerov sindrom tip 1 (4k25)<\/li>\n<li style=\"text-align: left;\">Saethre-Chotzen sindrom (7p21.1)<\/li>\n<li style=\"text-align: left;\">Gubitak sluha &#8211; sindrom neplodnosti (15k15.3)<\/li>\n<li style=\"text-align: left;\">Smit-Magenisov sindrom (17p11.2)<\/li>\n<li style=\"text-align: left;\">Malformacija rascepa \u0161aka-stopalo tip 5 (2k31)<\/li>\n<li style=\"text-align: left;\">Malformacija rascepa \u0161aka-stopalo tip 3 (10k24)<\/li>\n<li style=\"text-align: left;\">Trihorhinofalangealni sindrom tip 1 (8p23.3)<\/li>\n<li style=\"text-align: left;\">Van der Voude sindrom 1 (1k32.2-k41)<\/li>\n<li style=\"text-align: left;\">Vilmsov tumor tip 1 (11p13)<\/li>\n<li style=\"text-align: left;\">Ks-vezan limfoproliferativni sindrom (Ksk25)<\/li>\n<li style=\"text-align: left;\">Ksp11.22-p11.23 Sindrom dupliranja<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Koriste\u0107i uzorak krvi majke, RapidNIPT analizira bebin genetski materijal i procenjuje\u00a0hromozomske abnormalnosti. Za detaljne informacije o RapidNIPT-u, mo\u017eete pratiti vezu <a href=\"https:\/\/genoks.com.tr\/rapidnipt-hangi-hastaliklari-tarar\/\" target=\"_blank\" rel=\"noopener noreferrer\">\u0160ta je RapidNIPT?<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Patentirani NIPT test Genoksovog centra za procenu genetskih bolesti (Koliko je potrebno da se Genoks test objavi?) RapidNIPT se prijavljuje u roku od 3 radna dana. U nekim slu\u010dajevima, ovaj period se mo\u017ee produ\u017eiti do 5 radnih dana. \u0160ta je<span class=\"excerpt-hellip\"> [\u2026]<\/span><\/p>\n","protected":false},"author":2,"featured_media":1255,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"image","meta":{"footnotes":""},"categories":[145,1],"tags":[140,141,142,143],"class_list":["post-2417","post","type-post","status-publish","format-image","has-post-thumbnail","hentry","category-genel","category-uncategorized-tr","tag-down-sendromu","tag-genoks-testi","tag-nipt","tag-rapidnipt","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=\"Patentirani NIPT test Genoksovog centra za procenu genetskih bolesti (Koliko je potrebno da se Genoks test objavi?) RapidNIPT se prijavljuje u roku od 3 radna dana. U nekim slu\u010dajevima, ovaj period se mo\u017ee produ\u017eiti do 5 radnih dana.\u0160ta je RapidNIPT?RapidNIPT je skrining test nove generacije koji otkriva 70 razli\u010ditih hromozomskih bolesti, koji se prou\u010dava epruvetom\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<meta name=\"author\" content=\"Sercan Kantarc\u0131\"\/>\n\t<link rel=\"canonical\" href=\"https:\/\/genoks.com.tr\/me\/genoks-testi-kac-gunde-cikar-me\/\" \/>\n\t<meta name=\"generator\" content=\"All in One SEO Pro (AIOSEO) 4.9.5.2\" \/>\n\t\t<meta property=\"og:locale\" content=\"en_US\" \/>\n\t\t<meta property=\"og:site_name\" content=\"Genoks Genetics | NIPT, Skrining Nosilaca, Onkogenetika i WES Usluge - Bacamo Svjetlost na Va\u0161e Gene!\" \/>\n\t\t<meta property=\"og:type\" content=\"article\" \/>\n\t\t<meta property=\"og:title\" content=\"Koliko dana je potrebno da se dobije Genok test? 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