{"id":9680,"date":"2024-08-22T09:45:48","date_gmt":"2024-08-22T09:45:48","guid":{"rendered":"https:\/\/www.ankaraplaystation.com.tr\/?page_id=9680"},"modified":"2024-08-29T14:48:55","modified_gmt":"2024-08-29T14:48:55","slug":"pgt-xromosoma-kasalliklari-va-kasalliklari-uchun","status":"publish","type":"page","link":"https:\/\/www.istanbuleku.uz\/ru\/davolash-usullari\/pgt-xromosoma-kasalliklari-va-kasalliklari-uchun\/","title":{"rendered":"PGT \u2013 xromosoma kasalliklari va kasalliklari uchun"},"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\/doctor-embryologist-places-embryos-in-special-stra-2023-11-27-04-51-45-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>PGT \u2013 xromosoma kasalliklari va kasalliklari uchun<\/h3>[vc_column_text css=&raquo;&raquo;]Xromosoma kasalliklari va bitta gen kasalliklar uchun ikkita alohida PGT tekshiruvi mavjud. Ushbu bo\u2019limda xromosoma kasalliklari uchun PGT jarayoni muhokama qilinadi.<\/p>\n<p>&nbsp;<\/p>\n<h2>Xromosoma kasalliklari uchun PGT testi nima?<\/h2>\n<p>PGT (Preimplantatsiya genetik diagnostikasi), bu laboratoriya sharoitida olingan embrionlarni onaning bachadoniga o\u2019tkazishtan oldin genetik testen o\u2019tkazish jarayoni.<\/p>\n<h2>Nima uchun PGT testi qo\u2019llaniladi?<\/h2>\n<p>Inson embrionida jami 46 (23 juft) xromosoma mavjud bo\u2019lib, ularning yarmi onadan, yarmi otadan keladi. Ona nomzodning yoshi, tizimli xromosoma buzilishi (translokatsiya va boshqalar) juftlardan birida bo\u2019lish va boshqa ba\u2019zi biologik va ekologik sabablarga qarab, embrionlarda sonli yoki tarkibiy buzilish xavfi ortishi mumkin.<\/p>\n<p>Ko\u2019pgina xromosoma anomaliyalari hayotga mos kelmaydi, ya\u2019ni ba\u2019zilari (trisomiya 13, 16,18,21,22; monosomiya X)ular embrion bosqichida yoki bachadonga yopishmasdan rivojlanishni to\u2019xtatish yoki bachadonga yopishkan embriyonlar omadsizlik bilan tugaydi, kichik bir qismini (microdeletion sindromi, X [tyorner sindromi monosomy] va trisomiya 21 [down sindrom]) dunyoga keladi va ba\u2019zi aqli zaiflik turli darajadagi birinchi o\u2019rinda turadigan ba\u2019zi kasalliklarga sabab bo\u2019ladi. PGT testining maqsadi-yuqorida aytib o\u2019tilgan xavf guruhlarida normal embrionlarni aniqlash va o\u2019tkazishdan so\u2019ng, homiladorlik tushish xavfini kamaytirish va EKU muvaffaqiyatini oshirishdir.<\/p>\n<h2>PGT testi kimga qo\u2019llaniladi?<\/h2>\n<p>Dunyo va mamlakatimizda IVF kasallari orasida tobora ko\u2019proq qo\u2019llaniladigan ushbu test, birinchi navbatda, xromosoma anomaliyalari bo\u2019lgan embrionlarni rivojlantirish xavfi yuqori bo\u2019lgan juftliklarda qo\u2019llanilishi tavsiya etiladi.<\/p>\n<p><strong>Xromosoma kasalliklariga PGT yondashuvi, masalan;<\/strong><\/p>\n<ul>\n<li>Yoshi katta ayollar,<\/li>\n<li>Takroriy homiladorlik yo\u2019qotishlar<\/li>\n<li>Bir necha bor muvaffaqiyatsiz bo\u2019lgan EKU mavjudligi,<\/li>\n<li>Ota-onalar nomzodida genetik kasallik tashuvchilar (translokatsiya, inversiya va boshqalar.)<\/li>\n<li>Og\u2019ir erkak bepushtlik,<\/li>\n<li>Xromosoma anomaliyasi bo\u2019lgan homiladorlik kechirgan juftliklarda tavsiya etilgan usul.<\/li>\n<\/ul>\n<h2>PGT testi qanday amalga oshiriladi?<\/h2>\n<p>PGT testi embrion rivojlanishining 3 yoki 5-kunida biopsiya tomonidan olingan hujayralar da amalga oshiriladi. Bugungi kunda ishlatiladigan muzlatish texnikasi va yetishtirish usullarining rivojlanishi bilan hozirgi kunda asosan blastotsist fazasiga (5. kuni yoki 6 kun) embrionlarda qo\u2019llaniladi, vitrinifikatsiya usullari bilan muzlatilgandan so\u2019ng, PGT testi natijasiga ko\u2019ra keyingi muolajada o\u2019tkazish amalga oshiriladi.<\/p>\n<p>Tajribali embriolog tomonidan amalga oshiriladigan va tegishli sharoitlar mavjud bo\u2019lganda embrionning muzlash jarayoni embrionlarning rivojlanish yoki homiladorlikni shakllantirish imkoniyatini kamaytirmaydi; aksincha, ko\u2019pgina ilmiy tadqiqotlar shuni ko\u2019rsatdiki, embrionlar muzlatilib bachadon dam olganda keyin o\u2019tkazilganda, yangi o\u2019tkazilgan muolajalarga nisbatan muvaffaqiyat qozonish ehtimoli ortadi.<\/p>\n<h2>PGT testida qaysi usullar qo\u2019llaniladi?<\/h2>\n<p>Bizning markazlarimiz; dunyoda eng yangi texnologiya bo\u2019lgan NGS (Next Generation Sequencing) texnikasi qo\u2019llaniladi. Ushbu usul yordamida qisqa vaqt ichida barcha mavjud xromosomalar, mozaika va xromosoma qismlarining nomutanosibligi tekshirilishi mumkin.<\/p>\n<h2>PGT testi narxi qanday?<\/h2>\n<p>Qonunda talab qilinganidek, PGT testi narxi haqidagi ma\u2019lumotni veb-saytimizda e\u2019lon qila olmaymiz. PGT testi haqida batafsil ma\u2019lumot olish va shifokorlarimiz bilan bepul konsultasya uchun biz bilan bog\u2019lanish formasini to\u2019ldirishingiz mumkin yoki\u00a0<strong>Toshkent : +998 55 512 22 21 ,\u00a0Samarqand : +998 95 061 61 61 ,\u00a0Urganch: +998 90 826 22 24 raqamlardan<\/strong>\u00a0biz bilan bog\u2019lanishingiz mumkin.[\/vc_column_text][\/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_column_text css=&raquo;&raquo;]Xromosoma kasalliklari va bitta gen kasalliklar uchun ikkita alohida PGT tekshiruvi mavjud. Ushbu bo\u2019limda xromosoma kasalliklari uchun PGT jarayoni muhokama qilinadi. &nbsp; Xromosoma kasalliklari uchun PGT testi nima? [&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-9680","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9680"}],"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=9680"}],"version-history":[{"count":2,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9680\/revisions"}],"predecessor-version":[{"id":10017,"href":"https:\/\/www.istanbuleku.uz\/ru\/wp-json\/wp\/v2\/pages\/9680\/revisions\/10017"}],"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=9680"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}