Sa\u011fl\u0131k alan\u0131ndaki teknolojik altyap\u0131s\u0131n\u0131 s\u00fcrekli geli\u015ftirerek hastalar\u0131na daha h\u0131zl\u0131 ve daha do\u011fru sa\u011fl\u0131k hizmeti sunmay\u0131 hedefleyen Dokuz Eyl\u00fcl \u00dcniversitesi, genetik analizlerde kullan\u0131lan y\u00fcksek kapasiteli DNA dizileme cihaz\u0131 NovaSeq 6000\u2019i b\u00fcnyesine kazand\u0131rd\u0131. DE\u00dc T\u0131p Fak\u00fcltesi T\u0131bbi Genetik Ana Bilim Dal\u0131 ve Genetik Hastal\u0131klar De\u011ferlendirme Merkezinde kullan\u0131lmaya ba\u015flanan cihaz, nadir hastal\u0131klar\u0131n te\u015fhis, tedavi ve izlem s\u00fcre\u00e7lerinde ileri genomik analiz imk\u00e2n\u0131 sunuyor.<\/p>\n
S\u00f6z konusu cihaz, mevcut bilgiler do\u011frultusunda \u00fcniversite hastaneleri aras\u0131nda yaln\u0131zca Dokuz Eyl\u00fcl \u00dcniversitesi b\u00fcnyesinde bulunma \u00f6zelli\u011fi ta\u015f\u0131yor. Bu yeni teknoloji, hem klinik hizmetlerde tan\u0131 h\u0131z\u0131n\u0131 art\u0131r\u0131yor hem de bilimsel ara\u015ft\u0131rmalara \u00f6nemli katk\u0131lar sa\u011fl\u0131yor.<\/p>\n
\u201cNAD\u0130R HASTALIKLARIN Y\u00dcZDE 80\u2019\u0130 GENET\u0130K K\u00d6KENL\u0130\u201d<\/b><\/p>\n
28 \u015eubat D\u00fcnya Nadir Hastal\u0131klar G\u00fcn\u00fc kapsam\u0131nda de\u011ferlendirmelerde bulunan Prof. Dr. Ahmet Okay \u00c7a\u011flayan, nadir hastal\u0131klar\u0131n k\u00fcresel \u00f6l\u00e7ekte \u00f6nemli bir halk sa\u011fl\u0131\u011f\u0131 sorunu oldu\u011funa dikkat \u00e7ekti.<\/p>\n
Prof. Dr. \u00c7a\u011flayan, nadir hastal\u0131klar\u0131n tan\u0131m\u0131n\u0131n \u00fclkeden \u00fclkeye farkl\u0131l\u0131k g\u00f6stermekle birlikte T\u00fcrkiye\u2019de yakla\u015f\u0131k her 2 bin ki\u015fiden birinde g\u00f6r\u00fcld\u00fc\u011f\u00fcn\u00fc belirterek, \u201cNadir hastal\u0131klar\u0131n toplamda yakla\u015f\u0131k 8 bin farkl\u0131 t\u00fcr\u00fc bulunmaktad\u0131r. Bu hastal\u0131klar d\u00fcnya n\u00fcfusunun yakla\u015f\u0131k y\u00fczde 6\u2019s\u0131n\u0131 etkilemekte olup, d\u00fcnya genelinde 400 milyondan fazla birey nadir hastal\u0131klarla ya\u015famaktad\u0131r. Avrupa\u2019da yakla\u015f\u0131k 30 milyon, \u00fclkemizde ise 5 ila 7 milyon aras\u0131nda nadir hastal\u0131\u011fa sahip birey oldu\u011fu tahmin edilmektedir. Nadir hastal\u0131klar\u0131n olu\u015fumunda genetik fakt\u00f6rler y\u00fczde 80 oran\u0131nda rol oynamaktad\u0131r. Bu hastal\u0131klar\u0131n y\u00fczde 70\u2019i \u00e7ocukluk d\u00f6neminde ortaya \u00e7\u0131kmakta ve \u00fclkemizde hastalar\u0131n yakla\u015f\u0131k \u00fc\u00e7te birinde ya\u015fam kayb\u0131na neden olabilmektedir,\u201d dedi.<\/p>\n
\u201c\u00dcN\u0130VERS\u0130TE HASTANELER\u0130 ARASINDA SADECE DE\u00dc\u2019DE VAR\u201d<\/b><\/p>\n
NovaSeq 6000 cihaz\u0131n\u0131n sa\u011flad\u0131\u011f\u0131 ileri teknoloji sayesinde tan\u0131 s\u00fcre\u00e7lerinde \u00f6nemli bir h\u0131z ve do\u011fruluk art\u0131\u015f\u0131 sa\u011fland\u0131\u011f\u0131n\u0131 ifade eden Prof. Dr. \u00c7a\u011flayan, \u015funlar\u0131 kaydetti:<\/p>\n
\u201cDE\u00dc b\u00fcnyesine kazand\u0131r\u0131lan bu ileri teknoloji sayesinde hastalar\u0131m\u0131za daha h\u0131zl\u0131 ve do\u011fru tan\u0131 koyabiliyoruz. Ayn\u0131 zamanda y\u00fcr\u00fctt\u00fc\u011f\u00fcm\u00fcz bilimsel ara\u015ft\u0131rmalarla b\u00f6lgesel ve ulusal d\u00fczeyde \u00f6nemli katk\u0131lar sunuyoruz. \u00dcniversite hastaneleri aras\u0131nda NovaSeq 6000 cihaz\u0131n\u0131n yaln\u0131zca Dokuz Eyl\u00fcl \u00dcniversitesinde bulunmas\u0131, nadir hastal\u0131klar\u0131n te\u015fhis, tedavi ve izlem s\u00fcre\u00e7lerinde g\u00fc\u00e7l\u00fc bir translasyonel genomik altyap\u0131ya sahip oldu\u011fumuzu g\u00f6stermektedir.\u201d<\/p>\n
YILDA 10 B\u0130N HASTA TEDAV\u0130 G\u00d6R\u00dcYOR<\/b><\/p>\n
Dokuz Eyl\u00fcl \u00dcniversitesi Genetik Hastal\u0131klar De\u011ferlendirme Merkezinin T.C. Sa\u011fl\u0131k Bakanl\u0131\u011f\u0131 taraf\u0131ndan ruhsatland\u0131r\u0131lm\u0131\u015f bir merkez oldu\u011funu belirten Prof. Dr. \u00c7a\u011flayan, merkezde tan\u0131, ara\u015ft\u0131rma ve genetik dan\u0131\u015fmanl\u0131k hizmetlerinin b\u00fct\u00fcnc\u00fcl bir yakla\u015f\u0131mla sunuldu\u011funu ifade etti.<\/p>\n
Genetik hastal\u0131klar\u0131n yaln\u0131zca bireyi de\u011fil t\u00fcm aileyi etkileyen sa\u011fl\u0131k sorunlar\u0131 oldu\u011funa dikkat \u00e7eken \u00c7a\u011flayan, \u201cMerkezimizde genetik tan\u0131, risk de\u011ferlendirmesi ve dan\u0131\u015fmanl\u0131k hizmetleri sunulmaktad\u0131r. Bug\u00fcne kadar yakla\u015f\u0131k 10 bin hastaya klinik de\u011ferlendirme yap\u0131lm\u0131\u015f, 5 bin genetik test ger\u00e7ekle\u015ftirilmi\u015ftir. Ayr\u0131ca \u0130zmir Biyot\u0131p ve Genom Merkezi ile y\u00fcr\u00fctt\u00fc\u011f\u00fcm\u00fcz multidisipliner \u00e7al\u0131\u015fmalar sayesinde nadir hastal\u0131klar\u0131n tan\u0131 ve tedavi s\u00fcre\u00e7lerinde bilimsel ve klinik kapasitemizi s\u00fcrekli geli\u015ftirmekteyiz,\u201d \u015feklinde konu\u015ftu.<\/p>\n
B\u0130L\u0130MSEL ARA\u015eTIRMA VE HASTA H\u0130ZMETLER\u0130NDE G\u00dc\u00c7L\u00dc ALTYAPI<\/b><\/p>\n
Dokuz Eyl\u00fcl \u00dcniversitesinin sa\u011fl\u0131k alan\u0131ndaki ileri teknoloji yat\u0131r\u0131mlar\u0131 hem hasta hizmetlerinin kalitesini art\u0131r\u0131yor hem de nadir hastal\u0131klar ba\u015fta olmak \u00fczere genetik temelli hastal\u0131klar\u0131n anla\u015f\u0131lmas\u0131 ve tedavisine y\u00f6nelik bilimsel ara\u015ft\u0131rmalara g\u00fc\u00e7l\u00fc bir zemin haz\u0131rl\u0131yor. \u00dcniversite, sahip oldu\u011fu ileri genomik teknolojiler ve uzman akademik kadrosuyla ulusal ve uluslararas\u0131 d\u00fczeyde sa\u011fl\u0131k bilimlerine katk\u0131 sunmay\u0131 s\u00fcrd\u00fcr\u00fcyor.<\/p>\n
\u00a0<\/p>\n
Kaynak: (BYZHA) Beyaz Haber Ajans\u0131<\/p>\n","protected":false},"excerpt":{"rendered":"
Sa\u011fl\u0131k alan\u0131ndaki teknolojik altyap\u0131s\u0131n\u0131 s\u00fcrekli geli\u015ftirerek hastalar\u0131na daha h\u0131zl\u0131 ve daha do\u011fru sa\u011fl\u0131k hizmeti sunmay\u0131 hedefleyen Dokuz Eyl\u00fcl \u00dcniversitesi, genetik analizlerde kullan\u0131lan y\u00fcksek kapasiteli DNA dizileme cihaz\u0131 NovaSeq 6000\u2019i b\u00fcnyesine kazand\u0131rd\u0131.<\/p>\n","protected":false},"author":1,"featured_media":53638,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[11],"tags":[3303,467,6714,1122,2666],"class_list":["post-53637","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-saglik","tag-genetik","tag-hasta","tag-nadir-hastaliklar","tag-tani","tag-yaklasik"],"_links":{"self":[{"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/posts\/53637","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/comments?post=53637"}],"version-history":[{"count":1,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/posts\/53637\/revisions"}],"predecessor-version":[{"id":53639,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/posts\/53637\/revisions\/53639"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/media\/53638"}],"wp:attachment":[{"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/media?parent=53637"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/categories?post=53637"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/bihavadis.com\/index.php\/wp-json\/wp\/v2\/tags?post=53637"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}