{"id":4668,"date":"2013-10-01T15:00:00","date_gmt":"2013-10-01T17:00:00","guid":{"rendered":"https:\/\/www.silutesnaujienos.lt\/lt\/spali-galimybe-nemokamai-issitirti-del-paveldimo-kruties-ir-kiausidziu-vezio\/"},"modified":"2013-10-01T15:00:00","modified_gmt":"2013-10-01T17:00:00","slug":"spali-galimybe-nemokamai-issitirti-del-paveldimo-kruties-ir-kiausidziu-vezio","status":"publish","type":"post","link":"https:\/\/www.silutesnaujienos.lt\/lt\/spali-galimybe-nemokamai-issitirti-del-paveldimo-kruties-ir-kiausidziu-vezio\/","title":{"rendered":"Spal\u012f &#8211; galimyb\u0117 nemokamai i\u0161sitirti d\u0117l paveldimo kr\u016bties ir kiau\u0161id\u017ei\u0173 v\u0117\u017eio"},"content":{"rendered":"<p><a target=\"_blank\" rel=\"caption[Tyrimai. Getty image nuotr.] noopener noreferrer\" class=\"jcepopup\" href=\"\/\/silutesnaujienos.lt\/images\/stories\/2013\/10\/120424065130-prostate-cancer-screening-blood-test-story-top.jpg\" data-rel=\"lightbox-gallery-ntezXnld\" data-rl_title=\"\" data-rl_caption=\"\" title=\"\"><img loading=\"lazy\" decoding=\"async\" style=\"margin: 5px; float: left;\" class=\"caption\" title=\"Tyrimai. Getty image nuotr.\" alt=\"120424065130-prostate-cancer-screening-blood-test-story-top\" src=\"\/\/silutesnaujienos.lt\/images\/stories\/2013\/10\/thumbnails\/thumb_120424065130-prostate-cancer-screening-blood-test-story-top.jpg\" height=\"230\" width=\"307\" \/><\/a><strong>Vilniaus universiteto ligonin\u0117s Santari\u0161ki\u0173 klinik\u0173 (VUL SK) mokslininkai nustat\u0117, kad daugiau kaip 20% kiau\u0161id\u017ei\u0173 v\u0117\u017eio ir apie 7% kr\u016bties v\u0117\u017eio atvej\u0173 Lietuvoje pasirei\u0161kia d\u0117l BRCA1 ir BRCA2 gen\u0173 mutacij\u0173, i\u0161 kuri\u0173 da\u017eniausiai pasitaiko devynios mutacijos.<\/strong><\/p>\n<p>Moterys, paveld\u0117jusios BRCA1\/2 gen\u0173 mutacijas, gali tur\u0117ti iki 70-80% kr\u016bties ir iki 50-60% kiau\u0161id\u017ei\u0173 v\u0117\u017eio rizik\u0105. Ta\u010diau atlikus onkogenetin\u012f BRCA1\/2 gen\u0173 tyrim\u0105 sergan\u010diam asmeniui ir nusta\u010dius patologin\u0119 mutacij\u0105, yra \u012fmanoma \u012fvertinti sveik\u0173 giminai\u010di\u0173 genetin\u0119 rizik\u0105 ir \u0161iuolaikin\u0117mis priemon\u0117mis i\u0161vengti \u0161i\u0173 klasting\u0173 lig\u0173 arba jas anksti diagnozuoti ir i\u0161gydyti.<\/p>\n<p>\u201eToks \u017einojimas i\u0161 ties\u0173 padeda aplenkti v\u0117\u017e\u012f &#8211; galima prisiminti aktor\u0117s Angelinos Jolie bei daugelio kit\u0173 pacien\u010di\u0173 s\u0117km\u0117s istorijas\u201c, &#8211; teigia gydytojas onkogenetikas dr. Ram\u016bnas Janavi\u010dius, konsultuojantis paveldimo v\u0117\u017eio sindromais sergan\u010dius pacientus VUL SK Konsultacin\u0117je poliklinikoje.<\/p>\n<p>Tam, kad onkogenetiniai tyrimai suteikt\u0173 daugiausiai naudos, labai svarbu, kad onkogenetinei konsultacijai pirmiausia b\u016bt\u0173 nukreipiamas tiriamas sergantysis asmuo.<\/p>\n<p>Jei \u0161eimoje nustatoma konkreti BRCA gen\u0173 mutacija, tuomet galima atlikti ir sveik\u0173 asmen\u0173 ikisimptomin\u012f tyrim\u0105.<\/p>\n<p>Nusta\u010dius patologin\u0119 mutacij\u0105 sveikam asmeniui, yra \u012fvertinama individuali rizika, sudaromas individualus steb\u0117senos ir patikros planas, siekiant anks\u010diau nustatyti galim\u0105 lig\u0105 ankstyvose stadijose ar \u0161iuolaikin\u0117mis profilaktin\u0117mis chirurgin\u0117mis priemon\u0117mis jos i\u0161vengti.<\/p>\n<p>Genetinis i\u0161tyrimas ir patyrusi\u0173 specialist\u0173 pagalba suteikia unikali\u0105 galimyb\u0119 kryptingai aktyviai veikti, u\u017ekertant keli\u0105 galimoms komplikacijoms, taip pat suma\u017einant ne\u017einomyb\u0117s nerim\u0105.<\/p>\n<p>\u201eKita vertus, jei \u0161eimoje patvirtintas genetinis defektas nenustatomas, tokie asmenys i\u0161vengia nereikaling\u0173 diagnostini\u0173 proced\u016br\u0173 ir tyrim\u0173. Deja, ne visi pacientai yra teisingai nukreipiami onkogenetin\u0117ms konsultacijoms ir i\u0161tyrimui\u201c, &#8211; sako R.Janavi\u010dius.<\/p>\n<p>Spal\u012f &#8211; paveldimo kr\u016bties ir kiau\u0161id\u017ei\u0173 v\u0117\u017eio \u017einomumo m\u0117nes\u012f &#8211; VUL SK Onkogenetikos ir paveldimo v\u0117\u017eio koordinavimo centras bei Paveldimo v\u0117\u017eio asociacija kvie\u010dia pacientus, kuriems buvo diagnozuotas kr\u016bties ar kiau\u0161id\u017ei\u0173 v\u0117\u017eys ir turintiems paveldimumo po\u017eymius nemokamai atlikti onkogenetinius da\u017eniausi\u0173 BRCA1 ir BRCA2 gen\u0173 mutacij\u0173 tyrimus bei konsultacijas &#8211; tam reikia u\u017epildyti internetin\u0119 form\u0105, kuri\u0105 galima rasti www.ONKO-FORMA.genetika.lt.<\/p>\n<p>Tiriami tie pacientai, kuriems:<\/p>\n<p>* diagnozuotas kiau\u0161id\u017ei\u0173\/kiau\u0161intaki\u0173 v\u0117\u017eio tipas: SEROZIN\u0116 PAPILIN\u0116 (ADENO);<\/p>\n<p>* KARCINOMA; diagnozuotas kr\u016bties ir kiau\u0161id\u017ei\u0173 v\u0117\u017eys;<\/p>\n<p>* diagnozuotas kr\u016bties v\u0117\u017eio tipas: TRIGUBAI NEIGIAMAS (ER-, PR-, HER2-) arba BAZALINIS;<\/p>\n<p>* diagnozuotas kr\u016bties v\u0117\u017eys iki 40-ies met\u0173 (imtinai);<\/p>\n<p>* diagnozuotas abiej\u0173 kr\u016bt\u0173 v\u0117\u017eys; diagnozuotas kr\u016bties v\u0117\u017eys VYRAMS.<\/p>\n<p>Siekiama atkreipti \u012fvairi\u0173 specialybi\u0173 gydytoj\u0173 ir pacient\u0173 d\u0117mes\u012f \u012f paveldimo v\u0117\u017eio po\u017eymius, pagal kuriuos pacientai gali b\u016bti nukreipiami gydytojo onkogenetiko konsultacijai.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Vilniaus universiteto ligonin\u0117s Santari\u0161ki\u0173 klinik\u0173 (VUL SK) mokslininkai nustat\u0117, kad daugiau kaip 20% kiau\u0161id\u017ei\u0173 v\u0117\u017eio ir apie 7% kr\u016bties v\u0117\u017eio atvej\u0173 Lietuvoje pasirei\u0161kia d\u0117l BRCA1 ir BRCA2 gen\u0173 mutacij\u0173, i\u0161 kuri\u0173 da\u017eniausiai pasitaiko devynios mutacijos. Moterys, paveld\u0117jusios BRCA1\/2 gen\u0173 mutacijas, gali tur\u0117ti iki 70-80% kr\u016bties ir iki 50-60% kiau\u0161id\u017ei\u0173 v\u0117\u017eio rizik\u0105. Ta\u010diau atlikus onkogenetin\u012f BRCA1\/2 [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[53],"tags":[],"class_list":["post-4668","post","type-post","status-publish","format-standard","category-sveikatos-saltinis"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Spal\u012f - galimyb\u0117 nemokamai i\u0161sitirti d\u0117l paveldimo kr\u016bties ir kiau\u0161id\u017ei\u0173 v\u0117\u017eio - \u0160ilut\u0117s naujienos<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.silutesnaujienos.lt\/lt\/spali-galimybe-nemokamai-issitirti-del-paveldimo-kruties-ir-kiausidziu-vezio\/\" \/>\n<meta property=\"og:locale\" content=\"lt_LT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Spal\u012f - galimyb\u0117 nemokamai i\u0161sitirti d\u0117l paveldimo kr\u016bties ir kiau\u0161id\u017ei\u0173 v\u0117\u017eio - \u0160ilut\u0117s naujienos\" \/>\n<meta property=\"og:description\" content=\"Vilniaus universiteto ligonin\u0117s Santari\u0161ki\u0173 klinik\u0173 (VUL SK) mokslininkai nustat\u0117, kad daugiau kaip 20% kiau\u0161id\u017ei\u0173 v\u0117\u017eio ir apie 7% kr\u016bties v\u0117\u017eio atvej\u0173 Lietuvoje pasirei\u0161kia d\u0117l BRCA1 ir BRCA2 gen\u0173 mutacij\u0173, i\u0161 kuri\u0173 da\u017eniausiai pasitaiko devynios mutacijos. Moterys, paveld\u0117jusios BRCA1\/2 gen\u0173 mutacijas, gali tur\u0117ti iki 70-80% kr\u016bties ir iki 50-60% kiau\u0161id\u017ei\u0173 v\u0117\u017eio rizik\u0105. 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Moterys, paveld\u0117jusios BRCA1\/2 gen\u0173 mutacijas, gali tur\u0117ti iki 70-80% kr\u016bties ir iki 50-60% kiau\u0161id\u017ei\u0173 v\u0117\u017eio rizik\u0105. 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