{"id":3243,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/mitochondrial-panel-en\/"},"modified":"2026-05-02T05:14:16","modified_gmt":"2026-05-02T05:14:16","password":"","slug":"mitochondrial-panel-en","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/en\/docs\/mitochondrial-panel-en\/","title":{"rendered":"What is the Whole Mitochondrial Panel? What does it Cover?"},"content":{"rendered":"<p><!--genoks-intro-en:start--><\/p>\n<p><strong>Whole Mitochondrial Panel.<\/strong> Comprehensive analysis of mitochondrial DNA (mtDNA) and ~150 nuclear-encoded mitochondrial-disease genes. mtDNA full sequencing detects point mutations and large deletions; heteroplasmy quantification is reported. Indicated in suspected mitochondrial disorders (MELAS, MERRF, LHON, Leigh syndrome, etc.) with multisystem involvement, lactic acidosis, or maternal inheritance pattern. Sample: blood + tissue (muscle preferred for tissue-specific heteroplasmy).<\/p>\n<p><!--genoks-intro-en:end--><\/p>\n<p style=\"text-align: justify\"><strong>T\u00fcm Mitokondriyal Panel Nedir?<\/strong><br \/>\nMitokondriyal DNA, \u00e7ekirdekte yer alan DNA&#8217;dan farkl\u0131 olarak mitokondride yer alan k\u00fc\u00e7\u00fck bir DNA par\u00e7as\u0131d\u0131r. Mitokondriyal hastal\u0131klar, mitokondriyal DNA&#8217;da meydana gelen genetik de\u011fi\u015fikliklerden kaynaklan\u0131r ve v\u00fccudun enerji \u00fcretme sistemini etkiler. Bu hastal\u0131klar, kas g\u00fc\u00e7s\u00fczl\u00fc\u011f\u00fc, n\u00f6rolojik sorunlar, kalp hastal\u0131klar\u0131 ve di\u011fer sa\u011fl\u0131k sorunlar\u0131na neden olabilir. Mitokondriyal Panel, bir ki\u015finin mitokondriyal DNA&#8217;s\u0131ndaki genlerin dizilimini inceleyen bir genetik testtir. Bu test, mitokondriyal DNA&#8217;daki \u00e7e\u015fitli genetik de\u011fi\u015fiklikleri tespit ederek, mitokondriyal hastal\u0131klar\u0131n tan\u0131s\u0131nda yard\u0131mc\u0131 olabilir.<\/p>\n<p><strong>Mitokondriyal Hastal\u0131klara \u00d6rnekler;<\/strong><\/p>\n<ul>\n<li>MERRF sendromu: S\u0131kl\u0131kla n\u00f6rolojik semptomlarla ortaya \u00e7\u0131kan bir mitokondriyal hastal\u0131kt\u0131r. Epileptik n\u00f6betler, kas zay\u0131fl\u0131\u011f\u0131 ve koordinasyon problemleri gibi semptomlar i\u00e7erir.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<ul>\n<li>LHON (Leber kal\u0131tsal optik n\u00f6ropati): Bu hastal\u0131k, g\u00f6rme kayb\u0131yla karakterizedir ve genellikle gen\u00e7 eri\u015fkinleri etkiler.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<ul>\n<li>MELAS sendromu: Bu hastal\u0131k, kas zay\u0131fl\u0131\u011f\u0131, g\u00f6rme problemleri, epileptik n\u00f6betler, zihinsel fonksiyon bozuklu\u011fu ve di\u011fer semptomlar gibi bir dizi n\u00f6rolojik semptomlarla ili\u015fkilidir.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<ul>\n<li>NARP sendromu: N\u00f6rolojik bozukluklar, kas zay\u0131fl\u0131\u011f\u0131 ve epileptik n\u00f6betler gibi semptomlarla karakterizedir.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<ul>\n<li>Pearson sendromu: Bu hastal\u0131k, kan h\u00fccrelerinin \u00fcretimindeki sorunlardan kaynaklan\u0131r ve anemi, trombositopeni ve kemik ili\u011fi yetmezli\u011fi gibi semptomlar i\u00e7erir.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<table>\n<tbody>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>NGS<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>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>&#8220;Hasta Onam Formu&#8221;<\/strong> ve <strong>&#8220;KVKK Formu&#8221;<\/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=&#8221;710&#8243; title=&#8221;genetik ba\u015fvuru&#8221;]<\/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>Whole Mitochondrial Panel. Comprehensive analysis of mitochondrial DNA (mtDNA) and ~150 nuclear-encoded mitochondrial-disease genes. mtDNA full sequencing detects point mutations and large deletions; heteroplasmy quantification is reported. Indicated in suspected mitochondrial disorders (MELAS, MERRF, LHON, Leigh syndrome, etc.) with multisystem<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":[204],"doc_tag":[88,105,106,114,116,122],"class_list":["post-3243","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests","doc_tag-all-coding-exons","doc_tag-kalitsal","doc_tag-kanser","doc_tag-mitokondriyal-panel","doc_tag-mutasyon","doc_tag-postnatal"],"aioseo_notices":[],"year_month":"2026-05","word_count":403,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/en\/author\/admin\/"},"doc_category_info":[{"term_name":"Genoks GDHM Genetic Tests","term_url":"https:\/\/genoks.com.tr\/en\/docs-category\/genoks-gdhm-genetic-tests\/"}],"doc_tag_info":[{"term_name":"All Coding Exons)","term_url":"https:\/\/genoks.com.tr\/docs-tag\/all-coding-exons\/"},{"term_name":"Kal\u0131tsal","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kalitsal\/"},{"term_name":"kanser","term_url":"https:\/\/genoks.com.tr\/docs-tag\/kanser\/"},{"term_name":"Mitokondriyal Panel","term_url":"https:\/\/genoks.com.tr\/docs-tag\/mitokondriyal-panel\/"},{"term_name":"Mutasyon","term_url":"https:\/\/genoks.com.tr\/docs-tag\/mutasyon\/"},{"term_name":"Postnatal","term_url":"https:\/\/genoks.com.tr\/docs-tag\/postnatal\/"}],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"Whole Mitochondrial Panel. 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Indicated in suspected mitochondrial disorders (MELAS, MERRF, LHON, Leigh syndrome, etc.) with multisystem involvement, lactic acidosis, or maternal inheritance pattern. Sample: blood + tissue (muscle preferred for tissue-specific","twitter:creator":"@Genoks_GHTM","twitter:image":"https:\/\/genoks.com.tr\/wp-content\/uploads\/2025\/06\/genoks.svg"},"aioseo_meta_data":{"post_id":"3243","title":null,"description":null,"keywords":null,"keyphrases":null,"primary_term":null,"canonical_url":null,"og_title":null,"og_description":null,"og_object_type":"default","og_image_type":"default","og_image_url":null,"og_image_width":null,"og_image_height":null,"og_image_custom_url":null,"og_image_custom_fields":null,"og_video":null,"og_custom_url":null,"og_article_section":null,"og_article_tags":null,"twitter_use_og":false,"twitter_card":"default","twitter_image_type":"default","twitter_image_url":null,"twitter_image_custom_url":null,"twitter_image_custom_fields":null,"twitter_title":null,"twitter_description":null,"schema":{"blockGraphs":[],"customGraphs":[],"default":{"data":{"Article":[],"Course":[],"Dataset":[],"FAQPage":[],"Movie":[],"Person":[],"Product":[],"ProductReview":[],"Car":[],"Recipe":[],"Service":[],"SoftwareApplication":[],"WebPage":[]},"graphName":"","isEnabled":true},"graphs":[]},"schema_type":"default","schema_type_options":null,"pillar_content":false,"robots_default":true,"robots_noindex":false,"robots_noarchive":false,"robots_nosnippet":false,"robots_nofollow":false,"robots_noimageindex":false,"robots_noodp":false,"robots_notranslate":false,"robots_max_snippet":null,"robots_max_videopreview":null,"robots_max_imagepreview":"large","priority":null,"frequency":null,"local_seo":null,"seo_analyzer_scan_date":"2026-05-02 05:42:21","breadcrumb_settings":null,"limit_modified_date":false,"reviewed_by":null,"open_ai":null,"ai":null,"created":"2026-05-01 14:34:34","updated":"2026-05-02 05:42:21"},"aioseo_breadcrumb":"<div class=\"aioseo-breadcrumbs\"><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/genoks.com.tr\/en\/\" title=\"Home\">Home<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/genoks.com.tr\/en\/Genoks\/\" title=\"Dok\u00fcmanlar\">Dok\u00fcmanlar<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\t<a href=\"https:\/\/genoks.com.tr\/en\/docs-category\/genoks-gdhm-genetic-tests\/\" title=\"Genoks GDHM Genetic Tests\">Genoks GDHM Genetic Tests<\/a>\n<\/span><span class=\"aioseo-breadcrumb-separator\">&raquo;<\/span><span class=\"aioseo-breadcrumb\">\n\tWhat is the Whole Mitochondrial Panel? 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