{"id":9662,"date":"2024-08-22T09:44:37","date_gmt":"2024-08-22T09:44:37","guid":{"rendered":"https:\/\/www.ankaraplaystation.com.tr\/?page_id=9662"},"modified":"2024-08-28T12:18:45","modified_gmt":"2024-08-28T12:18:45","slug":"ngs-keng-qamrovli-xromosoma-tekshiruvi","status":"publish","type":"page","link":"https:\/\/www.istanbuleku.uz\/ru\/davolash-usullari\/ngs-keng-qamrovli-xromosoma-tekshiruvi\/","title":{"rendered":"NGS \u2013 keng qamrovli xromosoma tekshiruvi"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row][vc_column]<img decoding=\"async\" src=\"https:\/\/www.istanbuleku.uz\/ru\/wp-content\/uploads\/2024\/08\/the-concept-of-pregnancy-planning-ovulation-perio-2023-11-27-05-17-50-utc-scaled.jpg\" class=\"alignnone image-rounded \" alt=\"Image\"\/>[\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&raquo;50px&raquo;][\/vc_column][\/vc_row][vc_row][vc_column]<h3>NGS nima?<\/h3>[vc_separator color=&raquo;custom&raquo; align=&raquo;align_left&raquo; border_width=&raquo;2&#8243; el_width=&raquo;20&#8243; accent_color=&raquo;#f0f0f0&#8243;][vc_column_text css=&raquo;&raquo;]NGS (Next Generation Sequencing), embrionlarda keng qamrovli xromosoma tekshiruvi amalga oshirishga imkon beruvchi eng yangi ishlab chiqilgan genetik tahlil texnologiyasidir. NGS yordamida embrionlar tez va samarali tekshiriladi va embrionni o\u2019tkazilishidan oldin xromosoma darajasidagi genetik muammolar aniqlanadi. EKU muolajalarida olingan embrionlar bachadonga muvaffaqiyatli yopishsa ham, sog\u2019lom homilador bo\u2019lmaslikning muhim sabablaridan biri bu embrionlarda yuzaga keladigan xromosoma kasalliklaridir.<\/p>\n<p>NGS usuli bilan bajariladigan har tomonlama xromosoma tekshiruvi embrionlarda aytib o\u2019tilgan xromosoma buzilishlarini aniqlashda juda muhim rol o\u2019ynaydi. Ayniqsa, takroriy homiladorlik yo\u2019qatish va 40 yoshdan oshgan ayollarda, NGS usuli yordamida xromosoma sog\u2019lom ekanligi aniqlangan embrionni transplantatsiya qilish orqali yuqori homiladorlik muvaffaqiyatiga erishishimiz mumkin.[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&raquo;20px&raquo;][\/vc_column][\/vc_row][vc_row][vc_column]<h3>NGS kimga qo\u2019llaniladi?<\/h3>[vc_separator color=&raquo;custom&raquo; align=&raquo;align_left&raquo; border_width=&raquo;2&#8243; el_width=&raquo;20&#8243; accent_color=&raquo;#f0f0f0&#8243;][vc_column_text css=&raquo;&raquo;]EKU davolashda NGS texnikasi yordamida har tomonlama xromosoma tekshiruvi ba\u2019zi mamlakatlarda ishlatilishi keng tarqalgan bo\u2019lsa ham, Bah\u00e7eci Sog\u2019liqni saqlash guruhi sifatida, biz ayniqsa, quyidagi hollarda bu usul qo\u2019llaniladi:<\/p>\n<ul>\n<li>40 yoshdan oshgan ayollarga<\/li>\n<li>Sababi noma\u2019lum bo\u2019lgan bepushtlik holatlari<\/li>\n<li>Davolashning takroriy muvaffaqiyatsizligi<\/li>\n<li>Takroriy homiladorlikni yo\u2019qotish<\/li>\n<li>Og\u2019ir erkak bepushtligi<\/li>\n<\/ul>\n<h2>NGS texnikasining afzalliklari nimada?<\/h2>\n<p>Embrionni tashkil etuvchi barcha xromosomalarni keng tekshirish mumkin.<\/p>\n<p>Bu tekshirilgan hujayralardagi xromosomalarning soni va tarkibiy farqlarini aniqroq aniqlashimizga imkon beradi. Shunday qilib, bu \u201cmozaika\u201d deb nomlangan va turli xil xromosoma tuzilmalarini o\u2019z ichiga oladigan embrionlarni aniqlashda va davolash maqsadlarda ishlatilishi mumkin.<\/p>\n<p>NGS nafaqat gen kasalliklarini, xromosoma darajasidagi xatolarni ham o\u2019rganish imkoniyatini taqdim etadi. Tegishli sharoitlarda mavjud bo\u2019lgan yagona gen kasalliklarini tahlil qilish va HLA tipiklashtirish bilan bir vaqtda har tomonlama xromosoma ko\u2019rish imkonini beradi.[\/vc_column_text][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&raquo;40px&raquo;][\/vc_column][\/vc_row][vc_row][vc_column]<div class=\"dt-sc-title  title-center  sep-top dt-sc-simple-title \"><h2>Sizni klinikamizda kutamiz<\/h2><\/div>[vc_media_grid css=&raquo;&raquo; grid_id=&raquo;vc_gid:1724847460251-619afc01-ddcd-8&#8243; include=&raquo;9962,9903,9897,9892,9891,9890,9888&#8243;][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&raquo;50px&raquo;][\/vc_column][\/vc_row][vc_row][vc_column][vc_separator color=&raquo;custom&raquo; align=&raquo;align_left&raquo; border_width=&raquo;2&#8243; el_width=&raquo;20&#8243; accent_color=&raquo;#f0f0f0&#8243;][vc_column_text css=&raquo;&raquo;]NGS (Next Generation Sequencing), embrionlarda keng qamrovli xromosoma tekshiruvi amalga oshirishga imkon beruvchi eng yangi ishlab chiqilgan genetik tahlil texnologiyasidir. NGS yordamida embrionlar [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":9646,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"tpl-sidenavigation.php","meta":{"footnotes":""},"class_list":["post-9662","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9662"}],"collection":[{"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/comments?post=9662"}],"version-history":[{"count":3,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9662\/revisions"}],"predecessor-version":[{"id":9986,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9662\/revisions\/9986"}],"up":[{"embeddable":true,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9646"}],"wp:attachment":[{"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/media?parent=9662"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}