{"id":3305,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/irida-sr\/"},"modified":"2026-05-02T05:14:20","modified_gmt":"2026-05-02T05:14:20","password":"","slug":"irida-sr","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/sr\/docs\/irida-sr\/","title":{"rendered":"Anemija usled deficita gvo\u017e\u0111a rezistentna na gvo\u017e\u0111e"},"content":{"rendered":"<p><!--genoks-intro-sr:start--><\/p>\n<p><strong>Anemija usled deficita gvo\u017e\u0111a rezistentna na gvo\u017e\u0111e (IRIDA).<\/strong> Autozomno recesivna bolest izazvana mutacijama u TMPRSS6 genu koji kodira matriptaza-2, \u0161to dovodi do neprikladnog pove\u0107anja hepcidina i poreme\u0107ene apsorpcije gvo\u017e\u0111a u duodenumu. Klini\u010dka obele\u017eja: mikrocitna hipohromna anemija koja ne reaguje na oralno gvo\u017e\u0111e, delimi\u010dan odgovor na parenteralno gvo\u017e\u0111e. Dijagnoza: TMPRSS6 sekvenciranje + povi\u0161en omer hepcidin\/feritin u serumu. Upravljanje: parenteralno gvo\u017e\u0111e uz redovno hematolo\u0161ko pra\u0107enje.<\/p>\n<p><!--genoks-intro-sr:end--><\/p>\n<p style=\"text-align: justify\"><strong>Demir Diren\u00e7li Demir Eksikli\u011fi Anemisi Nedir?<\/strong><br \/>\nDemir diren\u00e7li demir eksikli\u011fi anemisi (DDDEA), demir eksikli\u011fi anemisine benzer semptomlar g\u00f6steren bir kan bozuklu\u011fudur. Bu durum, v\u00fccudun demir depolama mekanizmas\u0131n\u0131n bozulmas\u0131 nedeniyle olu\u015fur ve normalde demir takviyesi ile tedavi edilebilen standart demir eksikli\u011fi anemisine yan\u0131t vermez. DDDEA, demir eksikli\u011fi anemisi olan hastalar\u0131n %1-3&#8217;\u00fcnde g\u00f6r\u00fclebilir ve genellikle kal\u0131tsal bir hastal\u0131kt\u0131r. TMPRSS6 genindeki mutasyonlar Demir Diren\u00e7li Demir Eksikli\u011fi Anemisine neden olur<\/p>\n<p style=\"text-align: justify\">DDDEA&#8217;n\u0131n semptomlar\u0131 aras\u0131nda halsizlik, yorgunluk, nefes darl\u0131\u011f\u0131, cilt soluklu\u011fu, ta\u015fikardi (h\u0131zl\u0131 kalp at\u0131\u015f\u0131) ve ba\u015f d\u00f6nmesi gibi anemi semptomlar\u0131 yer al\u0131r. Ancak, standart demir eksikli\u011fi anemisine yan\u0131t vermeyen DDDEA hastalar\u0131 daha y\u00fcksek seviyelerde demir takviyelerine ihtiya\u00e7 duyabilirler veya daha agresif tedavi y\u00f6ntemleri gerektirebilirler.<\/p>\n<table>\n<tbody>\n<tr>\n<td><strong>Gen :<\/strong><\/td>\n<td>TMPRSS6<\/td>\n<\/tr>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>T\u00fcm Gen Dizi Analizi<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>6-8 Hafta (+\/- 2 Hafta)<\/td>\n<\/tr>\n<tr>\n<td><strong><strong>Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\n<td>Postnatal<\/td>\n<\/tr>\n<tr>\n<td><strong>Gerekli Numune<\/strong>:<\/td>\n<td>EDTA&#8217;l\u0131 Kan (2-4 ml)<\/td>\n<\/tr>\n<tr>\n<td><strong>Saklama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n<td>+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>T\u00fcm genetik testlerimiz <strong>&#8222;Hasta Onam Formu&#8220;<\/strong> ve <strong>&#8222;KVKK Formu&#8220;<\/strong>nun imzalanmas\u0131n\u0131n ard\u0131ndan \u00e7al\u0131\u015f\u0131lmaya ba\u015flan\u0131r.<\/p>\n<hr \/>\n<p><strong>Detayl\u0131 Bilgi Almak \u0130\u00e7in Bize Mesaj Atabilirsiniz.<\/strong><\/p>\n<table>\n<tbody>\n<tr>\n<td>[contact-form-7 id=&#8220;710&#8243; title=&#8220;genetik ba\u015fvuru&#8220;]<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Genoks Genetik Hastal\u0131klar De\u011ferlendirme Merkezi T.C. Sa\u011fl\u0131k Bankanl\u0131\u011f\u0131nca denetlenen ve GHDM-SM\/06.15\/01 ruhsat numaras\u0131 ile hizmet veren sa\u011fl\u0131k kurulu\u015fudur. genoks.com.tr web sayfas\u0131nda bulunan bilgiler, genetik de\u011ferlendirme ve\/veya tan\u0131-te\u015fhis ama\u00e7l\u0131 kullan\u0131lmamal\u0131d\u0131r. T\u00fcm i\u00e7erikler bilgilendirme ama\u00e7l\u0131d\u0131r.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Anemija usled deficita gvo\u017e\u0111a rezistentna na gvo\u017e\u0111e (IRIDA). Autozomno recesivna bolest izazvana mutacijama u TMPRSS6 genu koji kodira matriptaza-2, \u0161to dovodi do neprikladnog pove\u0107anja hepcidina i poreme\u0107ene apsorpcije gvo\u017e\u0111a u duodenumu. Klini\u010dka obele\u017eja: mikrocitna hipohromna anemija koja ne reaguje na<span class=\"excerpt-hellip\"> [\u2026]<\/span><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"doc_category":[208],"doc_tag":[],"class_list":["post-3305","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests-sr"],"aioseo_notices":[],"year_month":"2026-05","word_count":345,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/sr\/author\/admin\/"},"doc_category_info":[{"term_name":"\u0413\u0435\u043d\u0435\u0442\u0441\u043a\u0438 \u0442\u0435\u0441\u0442\u043e\u0432\u0438 Genoks GDHM","term_url":"https:\/\/genoks.com.tr\/sr\/docs-category\/genoks-gdhm-genetic-tests-sr\/"}],"doc_tag_info":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"Anemija usled deficita gvo\u017e\u0111a rezistentna na gvo\u017e\u0111e (IRIDA). 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Autozomno recesivna bolest izazvana mutacijama u TMPRSS6 genu koji kodira matriptaza-2, \u0161to dovodi do neprikladnog pove\u0107anja hepcidina i poreme\u0107ene apsorpcije gvo\u017e\u0111a u duodenumu. Klini\u010dka obele\u017eja: mikrocitna hipohromna anemija koja ne reaguje na oralno gvo\u017e\u0111e, delimi\u010dan odgovor na parenteralno gvo\u017e\u0111e. 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Autozomno recesivna bolest izazvana mutacijama u TMPRSS6 genu koji kodira matriptaza-2, \\u0161to dovodi do neprikladnog pove\\u0107anja hepcidina i poreme\\u0107ene apsorpcije gvo\\u017e\\u0111a u duodenumu. Klini\\u010dka obele\\u017eja: mikrocitna hipohromna anemija koja ne reaguje na oralno gvo\\u017e\\u0111e, delimi\\u010dan odgovor na parenteralno gvo\\u017e\\u0111e. 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