{"id":1504,"date":"2025-07-10T08:28:54","date_gmt":"2025-07-10T05:28:54","guid":{"rendered":"https:\/\/hastane2.omu.edu.tr\/?p=1504"},"modified":"2026-06-11T10:03:20","modified_gmt":"2026-06-11T07:03:20","slug":"tibbi-genetik","status":"publish","type":"post","link":"https:\/\/hastane.omu.edu.tr\/?p=1504","title":{"rendered":"T\u0131bbi Genetik"},"content":{"rendered":"\n<div class=\"wp-block-safirtema-mainheading singleHeading\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-takvim\"><use href=\"#safiricon-takvim\"><\/use><\/svg><\/div><div class=\"text\">T\u0131bbi Genetik Tarih\u00e7esi ve Hakk\u0131nda<\/div><\/div><\/div>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>T\u0131bbi Genetik Anabilim Dal\u0131<\/strong>, 04.11.2004 tarihli OM\u00dc senato karar\u0131 ve 17.12.2004 tarihli Y\u00d6K onay\u0131 ile 2005 y\u0131l\u0131nda Prof. Dr. G\u00f6n\u00fcl O\u011eUR ba\u015fkanl\u0131\u011f\u0131nda kurulmu\u015ftur. Anabilim dal\u0131 akademik kadrosunda \u00fc\u00e7 \u00f6\u011fretim \u00fcyesi ve bir ara\u015ft\u0131rma g\u00f6revlisi bulunmaktad\u0131r. Anabilim Dal\u0131na ait laboratuvarlar 09.11.2020 y\u0131l\u0131nda Sa\u011fl\u0131k Bakanl\u0131\u011f\u0131 taraf\u0131ndan Sitogenetik ve Molek\u00fcler alanlar\u0131 i\u00e7in GHDM-SM\/55.01\/01 ruhsat numaras\u0131 ile <strong>\u201cGenetik Hastal\u0131klar De\u011ferlendirme Merkezi\u201d<\/strong> olarak ruhsatland\u0131r\u0131larak faaliyet g\u00f6stermektedir. Merkezimiz, Karadeniz b\u00f6lgesi Samsun ilinde konu\u015flanm\u0131\u015f olmakla birlikte, b\u00f6lgedeki farkl\u0131 il ve il\u00e7elere hizmet vermektedir.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Genetik Hastal\u0131klar De\u011ferlendirme Merkezimizin hedefi germline ve\/veya somatik genetik de\u011fi\u015fikliklerin yol a\u00e7t\u0131\u011f\u0131 genetik hastal\u0131klar\u0131n klinik tan\u0131s\u0131n\u0131n konulmas\u0131, gerekli genetik testlerin yap\u0131lmas\u0131 ve hastaya genetik dan\u0131\u015fmanl\u0131k verilmesidir. Hastal\u0131k \u00f6zelinde yak\u0131n takiplerle hastalar\u0131m\u0131z\u0131n hayat kalitesinin artt\u0131r\u0131lmas\u0131, do\u011fabilecek komplikasyonlar\u0131n erken saptanarak \u00f6nlenmesi ve ailenin di\u011fer gebelikleri i\u00e7in tan\u0131 imk\u00e2nlar\u0131 sunulmas\u0131 hedeflenmektedir. Ayr\u0131ca t\u00fcm\u00f6rle ili\u015fkili genetik \u00e7al\u0131\u015fmalarla kanserlerin tan\u0131s\u0131n\u0131n desteklenmesi, prognostik fakt\u00f6rlerin belirlenmesi, ila\u00e7 se\u00e7imine katk\u0131 sunulmas\u0131 ve relapslar\u0131n erkenden belirlenmesi ama\u00e7lanmaktad\u0131r.<\/p>\n\n\n\n<div class=\"wp-block-safirtema-mainheading singleHeading mainHeading\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-mouse\"><use href=\"#safiricon-mouse\"><\/use><\/svg><\/div><div class=\"text\">M\u00fcracaat \u015eekli<\/div><\/div><\/div>\n\n\n\n<p class=\"wp-block-paragraph\">Poliklini\u011fimizde muayene olmak isteyen hastalar\u0131m\u0131z hastanemiz web sitesinden (<strong><a href=\"http:\/\/hastane.omu.edu.tr\" target=\"_blank\" rel=\"noopener\" title=\"\">http:\/\/hastane.omu.edu.tr<\/a><\/strong>) veya \u00e7a\u011fr\u0131 merkezimizden <strong>(0362 312 1955)<\/strong> randevu alarak muayene olabilmektedir.<\/p>\n\n\n\n<div class=\"wp-block-safirtema-mainheading singleHeading mainHeading\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-takim2\"><use href=\"#safiricon-takim2\"><\/use><\/svg><\/div><div class=\"text\">\u00d6\u011fretim \u00dcyeleri<\/div><\/div><\/div>\n\n\n\n<div class=\"\" data-col=\"2\"><ul class=\"wp-block-list\">\n<li><strong><a href=\"https:\/\/personel.omu.edu.tr\/tr\/ummet.abur\" target=\"_blank\" rel=\"noopener\" title=\"\">Dr. \u00d6\u011fr. \u00dcyesi \u00dcmmet ABUR&nbsp;<\/a><\/strong> <strong>Anabilim Dal\u0131 Ba\u015fkan\u0131<\/strong><\/li>\n\n\n\n<li><a href=\"https:\/\/personel.omu.edu.tr\/tr\/engin.altundag\" target=\"_blank\" rel=\"noopener\" title=\"\"><strong>Dr. \u00d6\u011fr. \u00dcyesi Engin ALTUNDA\u011e<\/strong><\/a><\/li>\n\n\n\n<li><a href=\"https:\/\/personel.omu.edu.tr\/tr\/omersalih.akar\" target=\"_blank\" rel=\"noopener\" title=\"\"><strong>Dr. \u00d6\u011fr. \u00dcyesi \u00d6mer Salih AKAR<\/strong><\/a><\/li>\n<\/ul><\/div>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>\u00d6zel Alan Bilgileri<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><a href=\"https:\/\/personel.omu.edu.tr\/tr\/ummet.abur\" target=\"_blank\" rel=\"noopener\" title=\"\">Dr. \u00d6\u011fr. \u00dcyesi \u00dcmmet ABUR<\/a><\/strong>: Hematogenetik, Tiroid Geneti\u011fi, \u0130nfertilite Geneti\u011fi, Prenatal Tan\u0131 Geneti\u011fi, Solid Kanser Geneti\u011fi<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/personel.omu.edu.tr\/tr\/engin.altundag\" target=\"_blank\" rel=\"noopener\" title=\"\"><strong>Dr. \u00d6\u011fr. \u00dcyesi Engin ALTUNDA\u011e<\/strong><\/a>: \u0130mm\u00fcnogenetik Hastal\u0131klar, Diyabet Geneti\u011fi, Hematogenetik, Prenatal Tan\u0131 Geneti\u011fi<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/personel.omu.edu.tr\/tr\/omersalih.akar\" target=\"_blank\" rel=\"noopener\" title=\"\"><strong>Dr. \u00d6\u011fr. \u00dcyesi \u00d6mer Salih AKAR<\/strong><\/a>: Kal\u0131tsal Kanser Sendromlar\u0131, Hematogenetik, N\u00f6rofibromatozis Geneti\u011fi, Benign Hematolojik Hastal\u0131klar (Talasemi) Geneti\u011fi, \u0130nfertilite Geneti\u011fi, Solid Kanser Geneti\u011fi<\/p>\n\n\n\n<div class=\"wp-block-safirtema-mainheading singleHeading mainHeading\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-noktalar\"><use href=\"#safiricon-noktalar\"><\/use><\/svg><\/div><div class=\"text\">Hizmet \u00d6zellikleri<\/div><\/div><\/div>\n\n\n\n<div class=\"\" data-col=\"1\"><ul class=\"wp-block-list\">\n<li>Geli\u015fmi\u015f Molek\u00fcler ve Sitogenetik Analizlerle Hassas Genetik Tan\u0131<\/li>\n\n\n\n<li>Kapsaml\u0131 Genetik Dan\u0131\u015fmanl\u0131k ve Risk Y\u00f6netimi<\/li>\n\n\n\n<li>Kal\u0131tsal Kanser Sendromlar\u0131 ve Farmakogenetik Uygulamalar\u0131<\/li>\n\n\n\n<li>Multidisipliner Klinik Entegrasyon ve Uzun D\u00f6nemli Takip<\/li>\n<\/ul><\/div>\n\n\n\n<div class=\"wp-block-safirtema-mainheading singleHeading mainHeading\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-soru\"><use href=\"#safiricon-soru\"><\/use><\/svg><\/div><div class=\"text\">S\u0131k\u00e7a Sorulanlar<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-safirtema-sorucevap safir-faq\"><div class=\"question\"><div class=\"safiricon icon\"><svg class=\"safiricon-soru\"><use href=\"#safiricon-soru\"><\/use><\/svg><\/div><span class=\"text\">T\u0131bbi Genetik Neler Yapar?<\/span><div class=\"openclose plus\"><\/div><\/div><p class=\"answer\">Bu anabilim dal\u0131, genetik hastal\u0131klar\u0131n tan\u0131 ve y\u00f6netimi i\u00e7in \u00e7e\u015fitli laboratuvar ve klinik uygulamalar\u0131 i\u00e7erir:<br><strong>Genetik Hastal\u0131klar\u0131n Tan\u0131s\u0131:<\/strong><br><strong>Kromozom Analizi (Karyotipleme):<\/strong> Down sendromu gibi say\u0131sal veya yap\u0131sal kromozom anormalliklerinin tespiti.<br><strong>Floresan \u0130n Situ Hibridizasyon (FISH):<\/strong> Kromozomlar\u0131n belirli b\u00f6lgelerindeki k\u00fc\u00e7\u00fck silinme veya eklenmelerin (mikrodelesyon\/mikroduplikasyon sendromlar\u0131) tespiti.<br><strong>Molek\u00fcler Genetik Testler:<\/strong> Tek gen hastal\u0131klar\u0131n\u0131n (\u00f6rn. kistik fibrozis, orak h\u00fccre anemisi, spinal m\u00fcsk\u00fcler atrofi &#8211; SMA) neden olan gen mutasyonlar\u0131n\u0131n DNA veya RNA d\u00fczeyinde belirlenmesi.<br><strong>Yeni Nesil Dizileme (NGS):<\/strong> Gen panelleri, t\u00fcm ekzom dizileme (WES) ve t\u00fcm genom dizileme (WGS) gibi y\u00fcksek verimli teknolojilerle y\u00fczlerce veya binlerce genin ayn\u0131 anda taranarak nedeni bilinmeyen kompleks genetik hastal\u0131klar\u0131n te\u015fhisi.<br><strong>Sitogenetik Mikroarray (Kromozomal Mikroarray):<\/strong> \u00c7ok k\u00fc\u00e7\u00fck kromozomal kopya say\u0131s\u0131 de\u011fi\u015fikliklerinin (CNV) t\u00fcm genom d\u00fczeyinde tespiti, geli\u015fimsel gecikme ve do\u011fumsal anomalilerin nedeni ara\u015ft\u0131rmas\u0131nda kullan\u0131l\u0131r.<br><strong>Kal\u0131tsal Kanser Sendromlar\u0131:<\/strong><br>Meme, yumurtal\u0131k (over), kolon gibi kanserlere genetik yatk\u0131nl\u0131k olu\u015fturan gen mutasyonlar\u0131n\u0131n (\u00f6rn. BRCA1\/2, Lynch sendromu genleri) tespiti ve bu ailelere y\u00f6nelik risk de\u011ferlendirmesi ve takip \u00f6nerileri.<br><strong>Genetik Dan\u0131\u015fmanl\u0131k:<\/strong><br>Genetik bir hastal\u0131\u011f\u0131 olan veya bu hastal\u0131\u011f\u0131n ta\u015f\u0131y\u0131c\u0131s\u0131 olan bireylere ve ailelerine hastal\u0131\u011f\u0131n do\u011fas\u0131, kal\u0131t\u0131m \u015fekli, tekrarlama riski, genetik test se\u00e7enekleri ve risk y\u00f6netimi konular\u0131nda bilgi ve destek sunmak.<br>Gebelik \u00f6ncesi veya s\u0131ras\u0131nda (prenatal tan\u0131) fet\u00fcsteki genetik risklerin de\u011ferlendirilmesi.<br>Evlilik \u00f6ncesi ta\u015f\u0131y\u0131c\u0131l\u0131k taramalar\u0131.<br><strong>Farmakogenetik:<\/strong><br>Bireylerin genetik yap\u0131lar\u0131n\u0131n, ila\u00e7lara verdikleri yan\u0131t\u0131 (etkinlik ve yan etki) nas\u0131l etkiledi\u011fini inceleyerek, ki\u015fiye \u00f6zel ila\u00e7 se\u00e7imi ve doz ayarlamas\u0131 i\u00e7in rehberlik etmek.<br><strong>Prenatal (Do\u011fum \u00d6ncesi) Tan\u0131:<\/strong><br>Amniyosentez, koryon villus biyopsisi gibi giri\u015fimsel y\u00f6ntemlerle veya anne kan\u0131ndan serbest fetal DNA analizi (NIPT) ile fet\u00fcsteki genetik anormalliklerin tespiti.<br><strong>Preimplantasyon Genetik Tan\u0131 (PGT):<\/strong><br>T\u00fcp bebek tedavisi (IVF) s\u0131ras\u0131nda embriyolar\u0131n rahme yerle\u015ftirilmeden \u00f6nce genetik hastal\u0131klar a\u00e7\u0131s\u0131ndan taranmas\u0131.<br><strong>Nadir Hastal\u0131klar Ara\u015ft\u0131rmas\u0131:<\/strong><br>Tan\u0131s\u0131 konulamayan, kompleks t\u0131bbi durumlar\u0131n genetik nedenlerini ara\u015ft\u0131rmak i\u00e7in ileri genetik testler uygulamak ve yorumlamak.<\/p><\/div>\n\n\n\n<div class=\"wp-block-safirtema-sorucevap safir-faq\"><div class=\"question\"><div class=\"safiricon icon\"><svg class=\"safiricon-soru\"><use href=\"#safiricon-soru\"><\/use><\/svg><\/div><span class=\"text\">Neden T\u0131bbi Genetik Anabilim Dal\u0131 \u00d6nemlidir?<\/span><div class=\"openclose plus\"><\/div><\/div><p class=\"answer\">Bu uzmanl\u0131k alan\u0131, hastal\u0131klar\u0131n k\u00f6kenindeki genetik fakt\u00f6rleri anlayarak, tan\u0131dan tedaviye ve \u00f6nlenmeye kadar uzanan s\u00fcre\u00e7lerde \u00e7\u0131\u011f\u0131r a\u00e7ar:<br><strong>Hastal\u0131klar\u0131n K\u00f6k Nedenini Belirleme:<\/strong> Bir\u00e7ok kronik ve nadir hastal\u0131\u011f\u0131n temelinde yatan genetik hatalar\u0131 tespit ederek, semptomatik tedavinin \u00f6tesinde hastal\u0131\u011f\u0131n ger\u00e7ek nedenini ortaya \u00e7\u0131kar\u0131r.<br><strong>Do\u011fru Tan\u0131 ve Ay\u0131r\u0131c\u0131 Tan\u0131:<\/strong> Benzer semptomlarla seyreden ancak genetik k\u00f6keni farkl\u0131 olan hastal\u0131klar\u0131 ay\u0131rt etmeye yard\u0131mc\u0131 olur, bu da do\u011fru tedavi ve y\u00f6netim i\u00e7in kritik \u00f6neme sahiptir.<br><strong>Tedavi ve Y\u00f6netime Y\u00f6nlendirme:<\/strong> Genetik tan\u0131, baz\u0131 durumlarda hastal\u0131\u011fa \u00f6zg\u00fc (hedefe y\u00f6nelik) tedavilerin se\u00e7ilmesine, komplikasyonlar\u0131n \u00f6nlenmesine veya uygun rehabilitasyon programlar\u0131n\u0131n planlanmas\u0131na rehberlik eder.<br><strong>Risk De\u011ferlendirmesi ve \u00d6nleme:<\/strong> Ailedeki genetik hastal\u0131k riskini belirleyerek, bireylerin ve ailelerin bilin\u00e7li kararlar almas\u0131na (\u00f6rn. aile planlamas\u0131, erken tarama programlar\u0131na kat\u0131lma) olanak tan\u0131r.<br><strong>Ki\u015fiselle\u015ftirilmi\u015f T\u0131p (Hassas T\u0131p):<\/strong> Her bireyin genetik yap\u0131s\u0131n\u0131n benzersiz oldu\u011funu kabul ederek, ila\u00e7 se\u00e7iminden doz ayarlamas\u0131na kadar tedavi yakla\u015f\u0131mlar\u0131n\u0131 ki\u015fiye \u00f6zel hale getirir.<br><strong>Psikososyal Destek:<\/strong> Genetik hastal\u0131k tan\u0131s\u0131 alan veya risk ta\u015f\u0131yan bireylere ve ailelere duygusal destek ve dan\u0131\u015fmanl\u0131k sa\u011flayarak, ya\u015fad\u0131klar\u0131 zorluklarla ba\u015fa \u00e7\u0131kmalar\u0131na yard\u0131mc\u0131 olur.<br><strong>Ara\u015ft\u0131rma ve \u0130novasyon:<\/strong> Genetik teknolojilerdeki h\u0131zl\u0131 geli\u015fmelerle birlikte, T\u0131bbi Genetik yeni tan\u0131 y\u00f6ntemlerinin geli\u015ftirilmesi ve gen terapileri gibi gelecekteki tedavi yakla\u015f\u0131mlar\u0131n\u0131n temelini olu\u015fturur.<\/p><\/div>\n\n\n\n<div class=\"wp-block-safirtema-sorucevap safir-faq\"><div class=\"question\"><div class=\"safiricon icon\"><svg class=\"safiricon-soru\"><use href=\"#safiricon-soru\"><\/use><\/svg><\/div><span class=\"text\">T\u0131bbi Genetik Uzman\u0131 Kimdir?<\/span><div class=\"openclose plus\"><\/div><\/div><p class=\"answer\">T\u0131bbi Genetik uzman\u0131, t\u0131p fak\u00fcltesini bitirdikten sonra <strong>T\u0131bbi Genetik Anabilim Dal\u0131nda<\/strong> uzmanl\u0131k e\u011fitimi (genellikle 4 y\u0131l) alm\u0131\u015f hekimdir. Bu kapsaml\u0131 e\u011fitim, kendilerine temel genetik, molek\u00fcler biyoloji, sitogenetik, biyoinformatik, genetik hastal\u0131klar\u0131n klinik \u00f6zellikleri, kal\u0131t\u0131m kal\u0131plar\u0131, genetik testlerin prensipleri ve yorumlanmas\u0131, genetik dan\u0131\u015fmanl\u0131k eti\u011fi ve uygulamalar\u0131 konular\u0131nda derinlemesine bilgi ve beceri kazand\u0131r\u0131r. Karma\u015f\u0131k genetik verileri analiz etme, test sonu\u00e7lar\u0131n\u0131 klinik bulgularla b\u00fct\u00fcnle\u015ftirme, aile a\u011fa\u00e7lar\u0131n\u0131 yorumlama, hasta ve ailelere anla\u015f\u0131l\u0131r dilde genetik bilgi aktarma, gizlilik ve etik prensiplere uyma, multidisipliner ekip \u00e7al\u0131\u015fmas\u0131na kat\u0131lma ve genetik teknolojilerdeki geli\u015fmeleri yak\u0131ndan takip etme yetene\u011fi bu alandaki hekimler i\u00e7in temel \u00f6zelliklerdir.<\/p><\/div>\n\n\n\n<div class=\"wp-block-safirtema-bgtext descriptionbox question\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-takim3\"><use href=\"#safiricon-takim3\"><\/use><\/svg><\/div><div class=\"header\">OM\u00dc T\u0131p Fak\u00fcltesi Sa\u011fl\u0131k Uygulama ve Ara\u015ft\u0131rma Merkezi<\/div><div class=\"content\">T\u0131bbi Genetik hakk\u0131nda t\u00fcm detayl\u0131 bilgilendirmeler a\u015fa\u011f\u0131da yap\u0131lm\u0131\u015ft\u0131r.<\/div><\/div><\/div>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Geli\u015fmi\u015f Molek\u00fcler ve Sitogenetik Analizlerle Hassas Genetik Tan\u0131<\/strong> <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">T\u0131bbi Genetik hizmetlerinin temelinde, insan genetik materyalindeki (DNA, RNA, kromozomlar) <strong>de\u011fi\u015fikliklerin en y\u00fcksek do\u011frulukla saptanmas\u0131<\/strong> i\u00e7in \u00e7e\u015fitli ileri laboratuvar analizleri yatar. Uzmanlar, kromozom anomalilerini tespit etmek i\u00e7in <strong>karyotipleme ve FISH<\/strong> gibi sitogenetik y\u00f6ntemleri kullan\u0131rken; tek gen hastal\u0131klar\u0131 veya kal\u0131tsal kanser yatk\u0131nl\u0131klar\u0131 i\u00e7in <strong>Yeni Nesil Dizileme (NGS)<\/strong>, PCR ve Sanger dizileme gibi molek\u00fcler genetik testleri uygularlar. Bu geli\u015fmi\u015f y\u00f6ntemler, genlerdeki nokta mutasyonlar\u0131ndan b\u00fcy\u00fck kromozomal yeniden d\u00fczenlenmelere kadar geni\u015f bir yelpazedeki genetik hatalar\u0131 belirleyerek, geli\u015fimsel gecikmeler, do\u011fumsal anomaliler, nadir sendromlar ve kal\u0131tsal kanserler gibi durumlar\u0131n kesin tan\u0131s\u0131na ula\u015f\u0131lmas\u0131n\u0131 sa\u011flar.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Kapsaml\u0131 Genetik Dan\u0131\u015fmanl\u0131k ve Risk Y\u00f6netimi<\/strong> <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Bu hizmetler, genetik hastal\u0131k tan\u0131s\u0131 alm\u0131\u015f, bu hastal\u0131klar i\u00e7in risk ta\u015f\u0131yan veya ta\u015f\u0131y\u0131c\u0131 konumunda olan bireylere ve ailelerine <strong>kapsaml\u0131 genetik dan\u0131\u015fmanl\u0131k<\/strong> sa\u011flamay\u0131 i\u00e7erir. T\u0131bbi Genetik uzmanlar\u0131, hastal\u0131\u011f\u0131n do\u011fas\u0131, kal\u0131t\u0131m \u015fekli, tekrarlama riski, genetik test se\u00e7enekleri (prenatal, preimplantasyon, do\u011fum sonras\u0131) ve olas\u0131 sonu\u00e7lar\u0131 hakk\u0131nda \u015feffaf ve anla\u015f\u0131l\u0131r bilgi sunarlar. Aile a\u011fa\u00e7lar\u0131n\u0131 analiz ederek riskleri de\u011ferlendirir ve bireylerin bilin\u00e7li kararlar almas\u0131na yard\u0131mc\u0131 olurlar. Bu s\u00fcre\u00e7, sadece t\u0131bbi bilgiyi aktarmakla kalmaz, ayn\u0131 zamanda ailelerin psikososyal ihtiya\u00e7lar\u0131n\u0131 da g\u00f6z \u00f6n\u00fcnde bulundurarak, etik ve duyarl\u0131 bir yakla\u015f\u0131m sergiler.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Kal\u0131tsal Kanser Sendromlar\u0131 ve Farmakogenetik Uygulamalar\u0131<\/strong> <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">T\u0131bbi Genetik Anabilim Dal\u0131, bireylerin kansere genetik yatk\u0131nl\u0131\u011f\u0131n\u0131 belirleyen <strong>kal\u0131tsal kanser sendromlar\u0131n\u0131n (\u00f6rn. BRCA1\/2 ile ili\u015fkili meme\/yumurtal\u0131k kanseri)<\/strong> tan\u0131s\u0131nda ve y\u00f6netilmesinde \u00f6nemli bir rol oynar. Ailedeki kanser \u00f6yk\u00fcs\u00fcn\u00fc de\u011ferlendirerek riskli bireylere genetik testler sunar ve pozitif \u00e7\u0131kan ta\u015f\u0131y\u0131c\u0131lara y\u00f6nelik takip programlar\u0131 (erken tarama, risk azalt\u0131c\u0131 cerrahi) konusunda rehberlik eder. Ayr\u0131ca, <strong>farmakogenetik<\/strong> alan\u0131nda, bireylerin genetik profillerine g\u00f6re ila\u00e7lara verdikleri yan\u0131t\u0131n (etkinlik ve yan etki) de\u011ferlendirilmesi ve b\u00f6ylece daha g\u00fcvenli ve etkili ila\u00e7 tedavilerinin ki\u015fiselle\u015ftirilmesi konusunda klinik hekimlere dan\u0131\u015fmanl\u0131k sa\u011flar.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Multidisipliner Klinik Entegrasyon ve Uzun D\u00f6nemli Takip<\/strong> <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Bu anabilim dal\u0131, genetik hastal\u0131klar\u0131n \u00e7ok \u00e7e\u015fitli organ sistemlerini etkilemesi nedeniyle g\u00fc\u00e7l\u00fc bir <strong>multidisipliner i\u015fbirli\u011fi<\/strong> gerektirir. T\u0131bbi Genetik uzmanlar\u0131; \u00e7ocuk doktorlar\u0131, n\u00f6rologlar, onkologlar, jinekologlar, dahiliye uzmanlar\u0131, endokrinologlar ve psikologlar gibi farkl\u0131 bran\u015flardan uzmanlarla yak\u0131n i\u015fbirli\u011fi i\u00e7inde \u00e7al\u0131\u015f\u0131rlar. Kompleks ve nadir hastal\u0131klar\u0131n tan\u0131s\u0131 ve y\u00f6netiminde ortak kons\u00fcltasyonlar d\u00fczenlerler. Ayr\u0131ca, genetik tan\u0131s\u0131 konmu\u015f hastalar\u0131n ve ailelerinin <strong>uzun d\u00f6nemli takibini<\/strong> yaparak, hastal\u0131\u011f\u0131n seyrindeki de\u011fi\u015fiklikleri izler, olas\u0131 komplikasyonlara kar\u015f\u0131 \u00f6nlemler al\u0131nmas\u0131na yard\u0131mc\u0131 olur ve ya\u015fam boyu destek hizmeti sunarak hastalar\u0131n b\u00fct\u00fcnc\u00fcl iyile\u015fme s\u00fcre\u00e7lerini desteklerler.<\/p>\n\n\n\n<div class=\"wp-block-safirtema-mainheading singleHeading\"><div class=\"inner\"><div class=\"icon safiricon\"><svg class=\"safiricon-telefon\"><use href=\"#safiricon-telefon\"><\/use><\/svg><\/div><div class=\"text\">\u0130leti\u015fim<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-8f761849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<div class=\"safir-list\" data-col=\"1\"><ul class=\"wp-block-list has-white-background-color has-background\">\n<li><strong>Departman Sekreteri: 2774<\/strong><\/li>\n\n\n\n<li><strong>Poliklinik\/ Randevu sekreteri: 3665<\/strong><\/li>\n\n\n\n<li><strong>Sonu\u00e7 Sekreteri: 3738<\/strong><\/li>\n\n\n\n<li><strong>Ondokuz May\u0131s \u00dcniversitesi Sa\u011fl\u0131k Uygulama ve Ara\u015ft\u0131rma Merkezi T\u0131bbi Genetik Anabilim Dal\u0131 55200 Atakum \/ Samsun<\/strong><\/li>\n\n\n\n<li><strong>Tel : 0 362 312 19 19<\/strong><\/li>\n\n\n\n<li><strong>Fax: 0 362 457 60 41<\/strong><\/li>\n<\/ul><\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<div style=\"border: 1px solid #ccc; border-radius: 5px; box-shadow: 2px 2px 5px #888888; padding: 10px;\">\n <iframe src=\"https:\/\/www.google.com\/maps\/embed?pb=!1m18!1m12!1m3!1d2994.111089551137!2d36.20858627654235!3d41.37167109696912!2m3!1f0!2f0!3f0!3m2!1i1024!2i768!4f13.1!3m3!1m2!1s0x40887eeddaf9f141%3A0x24561b910d5e11f3!2zT25kb2t1eiBNYXnEsXMgw5xuaXZlcnNpdGVzaSBUxLFwIEZha8O8bHRlc2k!5e0!3m2!1str!2str!4v1751288237149!5m2!1str!2str\" width=\"100%\" height=\"450\" style=\"border:0;\" allowfullscreen=\"\" loading=\"lazy\" referrerpolicy=\"no-referrer-when-downgrade\"><\/iframe>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>T\u0131bbi Genetik Anabilim Dal\u0131, 04.11.2004 tarihli OM\u00dc senato karar\u0131 ve 17.12.2004 tarihli Y\u00d6K onay\u0131 ile 2005 y\u0131l\u0131nda Prof. Dr. G\u00f6n\u00fcl O\u011eUR ba\u015fkanl\u0131\u011f\u0131nda kurulmu\u015ftur. Anabilim dal\u0131 akademik kadrosunda \u00fc\u00e7 \u00f6\u011fretim \u00fcyesi ve bir ara\u015ft\u0131rma g\u00f6revlisi bulunmaktad\u0131r. Anabilim Dal\u0131na ait laboratuvarlar 09.11.2020 y\u0131l\u0131nda Sa\u011fl\u0131k Bakanl\u0131\u011f\u0131 taraf\u0131ndan Sitogenetik ve Molek\u00fcler alanlar\u0131 i\u00e7in GHDM-SM\/55.01\/01 ruhsat numaras\u0131 ile \u201cGenetik Hastal\u0131klar [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":1506,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[518,4,687,685],"tags":[71,181,182],"class_list":["post-1504","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-ozellikli-birimlerimiz","category-bolumlerimiz","category-dahili-bolumler","category-ozellikli-birimler","tag-omu-genetik","tag-tibbi-genetik","tag-genetik"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/posts\/1504","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1504"}],"version-history":[{"count":9,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/posts\/1504\/revisions"}],"predecessor-version":[{"id":4423,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/posts\/1504\/revisions\/4423"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=\/wp\/v2\/media\/1506"}],"wp:attachment":[{"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1504"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1504"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/hastane.omu.edu.tr\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1504"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}