{"id":3222,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/genoks-tata-carrier-screening-en\/"},"modified":"2026-05-01T21:43:15","modified_gmt":"2026-05-01T21:43:15","password":"","slug":"genoks-tata-carrier-screening-en","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/en\/docs\/genoks-tata-carrier-screening-en\/","title":{"rendered":"Genoks TATA (Carrier Screening Test)"},"content":{"rendered":"<p><!--genoks-intro-en:start--><\/p>\n<p><strong>Genoks TATA \u2014 Expanded Carrier Screening Test<\/strong><\/p>\n<p>Carrier screening identifies individuals who carry a single copy of a recessive disease mutation without being affected themselves. The Genoks TATA panel screens hundreds of genes implicated in serious autosomal recessive and X-linked conditions (e.g. cystic fibrosis, SMA, beta-thalassemia, sickle cell disease, fragile X). When both partners carry the same recessive variant, each pregnancy carries a 25% risk of an affected child.<\/p>\n<p><strong>Best timing:<\/strong> preconception (before pregnancy). It can also be performed during pregnancy. <strong>Sample:<\/strong> 2-4 mL EDTA peripheral blood. <strong>Reporting:<\/strong> typically 4-6 weeks. A negative result reduces but does not eliminate risk; residual risk is communicated in the report. Couple-based testing is recommended in consanguineous unions and high-prevalence ethnic groups (e.g. Mediterranean for thalassemia).<\/p>\n<p><!--genoks-intro-en:end--><\/p>\n<p style=\"text-align: justify\"><strong>Ta\u015f\u0131y\u0131c\u0131 Nedir ?<\/strong><\/p>\n<p style=\"text-align: justify\">Genoks TATA, Genetik hastal\u0131k ta\u015f\u0131y\u0131c\u0131s\u0131, bir genetik hastal\u0131k i\u00e7in ta\u015f\u0131y\u0131c\u0131 olan, ancak hastal\u0131\u011f\u0131 kendisi g\u00f6stermeyen bir bireydir. Genetik hastal\u0131k ta\u015f\u0131y\u0131c\u0131s\u0131 olan bir ki\u015fi, hastal\u0131\u011f\u0131 kendisi g\u00f6stermese de, ta\u015f\u0131d\u0131\u011f\u0131 geni \u00e7ocuklar\u0131na ge\u00e7irebilir. Bu nedenle, \u00e7iftlerin aile planlamas\u0131 yaparken, genetik hastal\u0131klar\u0131n varl\u0131\u011f\u0131na dikkat etmeleri \u00f6nemlidir. E\u011fer bir \u00e7ift, her iki ebeveyn de bir genetik hastal\u0131k ta\u015f\u0131y\u0131c\u0131s\u0131 ise, \u00e7ocuklar\u0131n\u0131n bu hastal\u0131\u011fa yakalanma riski y\u00fcksek olabilir.<\/p>\n<p style=\"text-align: justify\">Genetik hastal\u0131klar, genetik materyalin (DNA) bir veya daha fazla genindeki mutasyonlar veya de\u011fi\u015fikliklerden kaynaklan\u0131r. Baz\u0131 genetik hastal\u0131klar, tek gen mutasyonlar\u0131na ba\u011fl\u0131d\u0131r, baz\u0131lar\u0131 ise birden fazla genin bir araya gelmesiyle ortaya \u00e7\u0131kar.<\/p>\n<p style=\"text-align: justify\">Baz\u0131 genetik hastal\u0131klar, erken tan\u0131 ve tedavi ile y\u00f6netilebilir veya tedavi edilebilirken, baz\u0131lar\u0131 maalesef hen\u00fcz tedavisi yoktur. Genetik hastal\u0131k ta\u015f\u0131y\u0131c\u0131l\u0131\u011f\u0131, hastal\u0131k riskinin azalt\u0131lmas\u0131 veya \u00f6nlenmesi i\u00e7in erken tan\u0131 ve tarama testleri yap\u0131lmas\u0131 gerekti\u011fini g\u00f6stermektedir.<\/p>\n<p><strong>GenoksTATA Test Se\u00e7enekleri<\/strong><\/p>\n<h6 style=\"text-align: justify\"><strong>GenoksTATA Mini Panel<\/strong><\/h6>\n<p style=\"text-align: justify\">GenoksTATA Mini <a href=\"https:\/\/genoks.com.tr\/docs\/spinal-muskuler-atrofi-sma-smn1-smn25q13-mlpa\/\" target=\"_blank\" rel=\"noopener\">Spinal M\u00fcsk\u00fcler Atrofi(SMA) <\/a> ve <a href=\"https:\/\/genoks.com.tr\/docs\/spinal-muskuler-atrofi-sma-smn1-smn25q13-mlpa\/\" target=\"_blank\" rel=\"noopener\">Kisitik Fibrozis<\/a> Hastal\u0131klar\u0131 taramas\u0131 yapmaktad\u0131r.<\/p>\n<table>\n<tbody>\n<tr>\n<td><strong><strong>Gen:<\/strong><\/strong><\/td>\n<td>SMN1 | SMN2 | 5q13 | CFTR<\/td>\n<\/tr>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>MLPA | Dizi analizi<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>SMA &#8211; 4 Hafta | CFTR &#8211; 4-6 Hafta<\/td>\n<\/tr>\n<tr>\n<td><strong><strong>Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\n<td>Postnatal<\/td>\n<\/tr>\n<tr>\n<td><strong>Gerekli Numune<\/strong>:<\/td>\n<td>EDTA&#8217;l\u0131 Kan (2-4 ml)<\/td>\n<\/tr>\n<tr>\n<td><strong>Saklama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n<td>+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h6 style=\"text-align: justify\"><strong>GenoksTATA MiniX Panel<\/strong><\/h6>\n<p style=\"text-align: justify\">GenoksTATA MiniX <a href=\"https:\/\/genoks.com.tr\/docs\/spinal-muskuler-atrofi-sma-smn1-smn25q13-mlpa\/\" target=\"_blank\" rel=\"noopener\">Spinal M\u00fcsk\u00fcler Atrofi(SMA) <\/a>, <a href=\"https:\/\/genoks.com.tr\/docs\/spinal-muskuler-atrofi-sma-smn1-smn25q13-mlpa\/\" target=\"_blank\" rel=\"noopener\">Kisitik Fibrozis<\/a> ve <a href=\"https:\/\/genoks.com.tr\/docs\/frajil-x-sendromu-300624-xe-bagli-dominant-frajil-x-sendromu-tekrar-sayisi\/\" target=\"_blank\" rel=\"noopener\">FrajiX<\/a> Hastal\u0131klar\u0131 taramas\u0131 yapmaktad\u0131r.<\/p>\n<hr \/>\n<table>\n<tbody>\n<tr>\n<td><strong><strong>Gen:<\/strong><\/strong><\/td>\n<td>CFTR |SMN1 | SMN2 | 5q13 | FMR1 | DMD<\/td>\n<\/tr>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>MLPA | Dizi analizi |Tekrar say\u0131s\u0131<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>SMA &#8211; 4 Hafta | CFTR &#8211; 4-6 Hafta | FrajilX &#8211; 4 Hafta | DMD &#8211; 4 Hafta<\/td>\n<\/tr>\n<tr>\n<td><strong><strong>Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\n<td>Postnatal<\/td>\n<\/tr>\n<tr>\n<td><strong>Gerekli Numune<\/strong>:<\/td>\n<td>EDTA&#8217;l\u0131 Kan (2-4 ml)<\/td>\n<\/tr>\n<tr>\n<td><strong>Saklamama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n<td>+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h6 style=\"text-align: justify\"><strong>GenoksTATA Maxi Panel<\/strong><\/h6>\n<p style=\"text-align: justify\">GenoksTATA Maxi 260 gende hastal\u0131k taramas\u0131 yapmaktad\u0131r.<\/p>\n<hr \/>\n<table>\n<tbody>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>NGS<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>8 Hafta (+\/- 2 Hafta)<\/td>\n<\/tr>\n<tr>\n<td><strong><strong>Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\n<td>Postnatal<\/td>\n<\/tr>\n<tr>\n<td><strong>Gerekli Numune<\/strong>:<\/td>\n<td>EDTA&#8217;l\u0131 Kan (2-4 ml)<\/td>\n<\/tr>\n<tr>\n<td><strong>Saklamama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n<td>+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>T\u00fcm genetik testlerimiz <strong>&#8220;Hasta Onam Formu&#8221;<\/strong> ve <strong>&#8220;KVKK Formu&#8221;<\/strong>nun imzalanmas\u0131n\u0131n ard\u0131ndan \u00e7al\u0131\u015f\u0131lmaya ba\u015flan\u0131r.<strong>Detayl\u0131 Bilgi Almak \u0130\u00e7in Bize Mesaj Atabilirsiniz.<\/strong><\/p>\n<table>\n<tbody>\n<tr>\n<td>[contact-form-7 id=&#8221;710&#8243; title=&#8221;genetik ba\u015fvuru&#8221;]<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Genoks Genetik Hastal\u0131klar De\u011ferlendirme Merkezi T.C. Sa\u011fl\u0131k Bankanl\u0131\u011f\u0131nca denetlenen ve GHDM-SM\/06.15\/01 ruhsat numaras\u0131 ile hizmet veren sa\u011fl\u0131k kurulu\u015fudur. genoks.com.tr web sayfas\u0131nda bulunan bilgiler, genetik de\u011ferlendirme ve\/veya tan\u0131-te\u015fhis ama\u00e7l\u0131 kullan\u0131lmamal\u0131d\u0131r. T\u00fcm i\u00e7erikler bilgilendirme ama\u00e7l\u0131d\u0131r.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Genoks TATA \u2014 Expanded Carrier Screening Test Carrier screening identifies individuals who carry a single copy of a recessive disease mutation without being affected themselves. The Genoks TATA panel screens hundreds of genes implicated in serious autosomal recessive and X-linked<span class=\"excerpt-hellip\"> [\u2026]<\/span><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"doc_category":[204],"doc_tag":[86,91,93,94,95,96,98,101,102,103,104,105,107,109,115,116,121,122,124,125,126,127,129,130,131,132],"class_list":["post-3222","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests","doc_tag-ailesel-akdeniz-atesi","doc_tag-array","doc_tag-cftr","doc_tag-cvs","doc_tag-dizi-analizi","doc_tag-dmd","doc_tag-duchenne-muskuler-distrofi","doc_tag-fmf","doc_tag-fmr1","doc_tag-frajil-x","doc_tag-frajil-x-sendromu","doc_tag-kalitsal","doc_tag-kistik-fibrozis","doc_tag-kromozom-analizi","doc_tag-mlpa","doc_tag-mutasyon","doc_tag-pcr","doc_tag-postnatal","doc_tag-sma","doc_tag-smn1","doc_tag-smn2","doc_tag-spinal-muskuler-atrofi","doc_tag-str-analizi","doc_tag-tek-gen-hastaligi","doc_tag-tek-nokta-mutasyon-analizitek-nokta-mutasyon-analizi","doc_tag-trombofili"],"aioseo_notices":[],"year_month":"2026-05","word_count":560,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/en\/author\/admin\/"},"doc_category_info":[{"term_name":"Genoks GDHM Genetic Tests","term_url":"https:\/\/genoks.com.tr\/en\/docs-category\/genoks-gdhm-genetic-tests\/"}],"doc_tag_info":[{"term_name":"Ailesel Akdeniz Ate\u015fi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/ailesel-akdeniz-atesi\/"},{"term_name":"array","term_url":"https:\/\/genoks.com.tr\/docs-tag\/array\/"},{"term_name":"CFTR","term_url":"https:\/\/genoks.com.tr\/docs-tag\/cftr\/"},{"term_name":"CVS","term_url":"https:\/\/genoks.com.tr\/docs-tag\/cvs\/"},{"term_name":"Dizi Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/dizi-analizi\/"},{"term_name":"DMD","term_url":"https:\/\/genoks.com.tr\/docs-tag\/dmd\/"},{"term_name":"Duchenne M\u00fcsk\u00fcler Distrofi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/duchenne-muskuler-distrofi\/"},{"term_name":"FMF","term_url":"https:\/\/genoks.com.tr\/docs-tag\/fmf\/"},{"term_name":"FMR1","term_url":"https:\/\/genoks.com.tr\/docs-tag\/fmr1\/"},{"term_name":"Frajil X","term_url":"https:\/\/genoks.com.tr\/docs-tag\/frajil-x\/"},{"term_name":"Frajil X Sendromu","term_url":"https:\/\/genoks.com.tr\/docs-tag\/frajil-x-sendromu\/"},{"term_name":"Kal\u0131tsal","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kalitsal\/"},{"term_name":"Kistik Fibrozis","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kistik-fibrozis\/"},{"term_name":"Kromozom Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kromozom-analizi\/"},{"term_name":"MLPA","term_url":"https:\/\/genoks.com.tr\/docs-tag\/mlpa\/"},{"term_name":"Mutasyon","term_url":"https:\/\/genoks.com.tr\/docs-tag\/mutasyon\/"},{"term_name":"PCR","term_url":"https:\/\/genoks.com.tr\/docs-tag\/pcr\/"},{"term_name":"Postnatal","term_url":"https:\/\/genoks.com.tr\/docs-tag\/postnatal\/"},{"term_name":"SMA","term_url":"https:\/\/genoks.com.tr\/docs-tag\/sma\/"},{"term_name":"SMN1","term_url":"https:\/\/genoks.com.tr\/docs-tag\/smn1\/"},{"term_name":"SMN2","term_url":"https:\/\/genoks.com.tr\/docs-tag\/smn2\/"},{"term_name":"Spinal M\u00fcsk\u00fcler Atrofi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/spinal-muskuler-atrofi\/"},{"term_name":"STR Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/str-analizi\/"},{"term_name":"Tek Gen Hastal\u0131\u011f\u0131","term_url":"https:\/\/genoks.com.tr\/docs-tag\/tek-gen-hastaligi\/"},{"term_name":"Tek Nokta Mutasyon AnaliziTek Nokta Mutasyon Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/tek-nokta-mutasyon-analizitek-nokta-mutasyon-analizi\/"},{"term_name":"Trombofili","term_url":"https:\/\/genoks.com.tr\/docs-tag\/trombofili\/"}],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"Genoks TATA \u2014 Expanded Carrier Screening TestCarrier screening identifies individuals who carry a single copy of a recessive disease mutation without being affected themselves. 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