{"id":28326,"date":"2022-08-22T01:00:15","date_gmt":"2022-08-21T22:00:15","guid":{"rendered":"https:\/\/nesiller.com\/nos-services\/"},"modified":"2023-05-05T17:25:47","modified_gmt":"2023-05-05T14:25:47","slug":"nos-services","status":"publish","type":"page","link":"https:\/\/nesiller.com\/fr\/nos-services\/","title":{"rendered":"NOS SERVICES"},"content":{"rendered":"\t\t
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\r\n 1.\tGenetik Dan\u0131\u015fmanl\u0131k<\/a>\r\n <\/h4>\r\n \r\n

Merkezimizde genetik hastal\u0131klarla ilgili olarak aile hikayesinin \u00e7\u0131kar\u0131lmas\u0131, fizik muayene ve destekleyici genetik testler ile hastaya tan\u0131 konulmas\u0131 ve genetik dan\u0131\u015fma konular\u0131nda hizmet vermekteyiz. Elde edilen genetik tan\u0131n\u0131n klini\u011fi, yani hastal\u0131\u011f\u0131n tan\u0131, tedavi ve bu s\u00fcreci nas\u0131l etkileyece\u011finin tart\u0131\u015f\u0131ld\u0131\u011f\u0131 genetik dan\u0131\u015fma seanslar\u0131d\u0131r. Kal\u0131tsal ge\u00e7i\u015fli yap\u0131daki genetik hastal\u0131klar\u0131n ve ko\u015fullar\u0131n hasta ve hasta yak\u0131nlar\u0131na aktar\u0131lmas\u0131 ama\u00e7lan\u0131r.\n\n\n\u2022\tSa\u011fl\u0131kl\u0131 \u00c7ocuk Sahibi Olma Dan\u0131\u015fmanl\u0131\u011f\u0131 \n\n1.\tKromozom anomalileri ve tek gen mutasyonlar\u0131\nTekrarlayan d\u00fc\u015f\u00fckler, hamilelik ba\u015far\u0131s\u0131zl\u0131klar\u0131, \u00f6l\u00fc do\u011fum veya do\u011fum sonras\u0131 tespit edilen anomalilerin en \u00f6nemli sebeplerinden biri genetiktir. Annede, babada veya her ikisinde bulunan kromozom anomalileri veya mutasyonlar embriyoya aktar\u0131larak geli\u015fen fet\u00fcste yap\u0131sal problemlere, dolayl\u0131 olarak da d\u00fc\u015f\u00fc\u011fe yol a\u00e7abilir (bkz. kromozomal an\u00f6ploidiler). Do\u011fumla sonu\u00e7lanan fakat mental ve\/veya fiziksel anomalilerle do\u011fam bebeklerde de genetik altyap\u0131 ilk ara\u015ft\u0131r\u0131lan fakt\u00f6rlerden biri olmal\u0131d\u0131r (bkz. Down Sendromu, SMA). Bu durumla kar\u015f\u0131la\u015fan veya ailesinde genetik hastal\u0131k \u00f6yk\u00fcs\u00fc olan bireylerin sa\u011fl\u0131kl\u0131 bir aile kurmak i\u00e7in genetik dan\u0131\u015fmanl\u0131k almas\u0131 \u00f6nerilmektedir.\n\n2.\tTeratojenite \nTeratojen kelimesi, malformasyonlu, anormal bebek do\u011fmas\u0131na neden olan maddelerin tan\u0131m\u0131 i\u00e7in kullan\u0131lmaktad\u0131r. Geli\u015fmi\u015f \u00fclkelerde bile fetal malformasyonlu bebeklerin do\u011fmas\u0131 normal \u00fcreme hayat\u0131n\u0131n bir \u00fcr\u00fcn\u00fc olarak tan\u0131mlan\u0131r ve t\u00fcm do\u011fumlar\u0131n %2\u2019sinde rastlan\u0131r. Teratojenite ise teratojen bir maddenin kullan\u0131m\u0131 sonucu bebekte meydana getirebilece\u011fi bozukluklard\u0131r. \n\nBiz Nesiller Genetik olarak hem hekimlere hem de gebelere teratojenler ve olas\u0131 etkileri ile ilgili dan\u0131\u015fmanl\u0131k hizmeti sunuyoruz. Teratojenite dan\u0131\u015fmanl\u0131\u011f\u0131 temelde bir risk ileti\u015fimidir. Ama\u00e7 gebeye riski mevcut verilerin \u0131\u015f\u0131\u011f\u0131nda do\u011fru bir \u015fekilde anlatabilmek ve daha da \u00f6nemlisi bu konuyu do\u011fru bir \u015fekilde anlayabilmesini sa\u011flamakt\u0131r.\n\n\n\u2022\tAkraba Evlili\u011fi Riskleri Dan\u0131\u015fmanl\u0131\u011f\u0131\n\nAkraba evlili\u011fi, genetik hastal\u0131klar\u0131n epidemolojisini etkileyen \u00f6nemli etmenlerden biridir ve \u00fclkemize %25\u2019in \u00fczerinde bulunmaktad\u0131r. Kal\u0131t\u0131mla ge\u00e7en hastal\u0131klar, gen ad\u0131 verilen kal\u0131t\u0131m maddesindeki de\u011fi\u015fimler ya da mutasyonlar sonucu ortaya \u00e7\u0131kar. T\u00fcm genlerimizden bir kopyas\u0131 anneden, bir kopyas\u0131 babadan olmak \u00fczere toplamda iki kopya bulunur. De\u011fi\u015fmi\u015f ya da bozulmu\u015f genlerden tek kopya olduklar\u0131nda dahi hastal\u0131\u011fa yol a\u00e7anlara dominant (bask\u0131n) genler, olu\u015fturduklar\u0131 hastal\u0131\u011fa ise dominant hastal\u0131k denir. Di\u011fer grup ise ancak \u00e7ift kopya olduklar\u0131nda hastal\u0131k ortaya \u00e7\u0131karabilen resesif (\u00e7ekinik) genlerdir, bunlar\u0131n neden olduklar\u0131 hastal\u0131klara ise resesif hastal\u0131klar denir. \u0130\u015fte akraba evliliklerinde veya kapal\u0131 toplumlarda bozuk genlerin bir araya gelme ihtimali daha y\u00fcksek oldu\u011fu i\u00e7in akraba evlili\u011finde genetik hastal\u0131klar, daha do\u011frusu resesif kal\u0131t\u0131mla ge\u00e7en hastal\u0131klar daha s\u0131k g\u00f6r\u00fcl\u00fcr.\n\nAkraba evlili\u011fi, zararl\u0131 bask\u0131n ve \u00e7ekinik genler \u00fcst \u00fcste gelerek \u00e7ak\u0131\u015fmas\u0131 olas\u0131l\u0131\u011f\u0131n\u0131 art\u0131rd\u0131\u011f\u0131ndan genetik hastal\u0131klar\u0131n g\u00f6r\u00fclmesine yol a\u00e7abilir. Bunlar\u0131n \u00e7ocukta g\u00f6r\u00fclmesi i\u00e7in anne ve baban\u0131n her ikisinin de en az\u0131ndan bir zararl\u0131 \u00e7ekinik gene sahip olmas\u0131 gerekir. Dolay\u0131s\u0131yla akraba evlilikleri; ayn\u0131 gen yap\u0131s\u0131na sahip olan ailede, \u00e7ekinik genlerin birbirleriyle kar\u015f\u0131la\u015fma olas\u0131l\u0131\u011f\u0131n\u0131 art\u0131racak ve anomalili \u00e7ocuklar\u0131 d\u00fcnyaya gelme ihtimalini ciddi \u015fekilde artt\u0131racakt\u0131r. \n\nNesiller, akraba evlili\u011fi yapm\u0131\u015f ya da yapmak \u00fczere olan \u00e7iftleri genetik yap\u0131lar\u0131na g\u00f6re de\u011ferlendirerek ailelerinde nelere dikkat etmeleri gerekti\u011fi konusunda onlar\u0131 bilgilendirmektedir.\n\n\u2022\tKad\u0131n ve Erkekte \u0130nfertilite (k\u0131s\u0131rl\u0131k) \n\u0130nfertilite, 35 ya\u015f alt\u0131 ki\u015filerin bir sene boyunca, 35 ya\u015f \u00fcst\u00fc ki\u015filerin ise 6 ay boyunca tekrarl\u0131 denemelere ra\u011fmen hamilelik ba\u015far\u0131zl\u0131\u011f\u0131 ile sonu\u00e7lanan durumlara denmektedir. Bu durum kad\u0131nlarda g\u00f6r\u00fclebilece\u011fi gibi erkeklerde de g\u00f6r\u00fclebilmektedir. Hamilelik sonras\u0131nda tekrarl\u0131 d\u00fc\u015f\u00fck ya\u015famak da infertilitenin bir belirtecidir. \n\u0130leri anne ya\u015f\u0131, sperm kusurlar\u0131, anatomik sebepler ve genetik hastal\u0131klar infertiliteye sebep olan ba\u015fl\u0131ca fakt\u00f6rlerdir. Genetik penceresinden bak\u0131ld\u0131\u011f\u0131nda; anne-baba adaylar\u0131nda bulunan kromozomal anomalilerin (kromozom say\u0131s\u0131nda farkl\u0131l\u0131k gibi) fet\u00fcse aktar\u0131lmas\u0131 d\u00fc\u015f\u00fckle sonu\u00e7lanabilirken; hamileli\u011fin hi\u00e7 olu\u015fmamas\u0131na sebebiyet veren Frajil X, Kistik Fibroz gibi genetik temelli hastal\u0131klar da oldu\u011fu bilinmektedir. \nKandan yap\u0131lacak genetik analizler ile olas\u0131 infertilite durumlar\u0131n\u0131z\u0131, genetik dan\u0131\u015fmanl\u0131k ile de ilerleyece\u011finiz yolu \u00f6\u011frenebilirsiniz.\n\n\u2022\tSa\u011fl\u0131kl\u0131 Ya\u015fam \nBu dan\u0131\u015fmanl\u0131k seanslar\u0131nda bireylerin genetik yap\u0131lar\u0131 g\u00f6z \u00f6n\u00fcnde bulundurularak ya\u015fam tarz\u0131, beslenme ve spor al\u0131\u015fkanl\u0131klar\u0131, yatk\u0131n olduklar\u0131 hastal\u0131klar ve olas\u0131 korunma y\u00f6ntemleri ile ilgili bilimsel tespitler ve \u00f6neriler sunulur. Bir bireyin sa\u011fl\u0131\u011f\u0131, bireyin genetik yap\u0131s\u0131 ve \u00e7evresel fakt\u00f6rlerin etkisi ile \u015fekillenir.<\/p>\r\n \r\n

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\r\n Blood Testing<\/a>\r\n <\/h4>\r\n \r\n

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\r\n Biochemistry<\/a>\r\n <\/h4>\r\n \r\n

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\r\n Histopatology<\/a>\r\n <\/h4>\r\n \r\n

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\r\n Microbioogy<\/a>\r\n <\/h4>\r\n \r\n

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\r\n Genetics<\/a>\r\n <\/h4>\r\n \r\n

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\r\n \r\n <\/i>READ MORE <\/a>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n<\/section>\r\n\r\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"

1. Genetik Dan\u0131\u015fmanl\u0131k Merkezimizde genetik hastal\u0131klarla ilgili olarak aile hikayesinin \u00e7\u0131kar\u0131lmas\u0131, fizik muayene ve destekleyici genetik testler ile hastaya tan\u0131 konulmas\u0131 ve genetik dan\u0131\u015fma konular\u0131nda hizmet vermekteyiz. Elde edilen genetik tan\u0131n\u0131n klini\u011fi, yani hastal\u0131\u011f\u0131n tan\u0131, tedavi ve bu s\u00fcreci nas\u0131l etkileyece\u011finin tart\u0131\u015f\u0131ld\u0131\u011f\u0131 genetik dan\u0131\u015fma seanslar\u0131d\u0131r. Kal\u0131tsal ge\u00e7i\u015fli yap\u0131daki genetik hastal\u0131klar\u0131n ve ko\u015fullar\u0131n hasta ve hasta […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-28326","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nNOS SERVICES - Nesiller Genetic Center<\/title>\n<meta name=\"description\" content=\"NOS SERVICES -\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/nesiller.com\/fr\/nos-services\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"NOS SERVICES\" \/>\n<meta property=\"og:description\" content=\"1. 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Genetik Dan\u0131\u015fmanl\u0131k Merkezimizde genetik hastal\u0131klarla ilgili olarak aile hikayesinin \u00e7\u0131kar\u0131lmas\u0131, fizik muayene ve destekleyici genetik testler ile hastaya tan\u0131 konulmas\u0131 ve genetik dan\u0131\u015fma konular\u0131nda hizmet vermekteyiz. Elde edilen genetik tan\u0131n\u0131n klini\u011fi, yani hastal\u0131\u011f\u0131n tan\u0131, tedavi ve bu s\u00fcreci nas\u0131l etkileyece\u011finin tart\u0131\u015f\u0131ld\u0131\u011f\u0131 genetik dan\u0131\u015fma seanslar\u0131d\u0131r. Kal\u0131tsal ge\u00e7i\u015fli yap\u0131daki genetik hastal\u0131klar\u0131n ve ko\u015fullar\u0131n hasta ve hasta\u2026","_links":{"self":[{"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/pages\/28326","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/comments?post=28326"}],"version-history":[{"count":3,"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/pages\/28326\/revisions"}],"predecessor-version":[{"id":29181,"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/pages\/28326\/revisions\/29181"}],"wp:attachment":[{"href":"https:\/\/nesiller.com\/fr\/wp-json\/wp\/v2\/media?parent=28326"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}