{"id":7396,"date":"2024-02-05T20:39:18","date_gmt":"2024-02-05T19:39:18","guid":{"rendered":"https:\/\/genetika-plzen.nullable.group\/?page_id=7396"},"modified":"2024-02-05T20:42:27","modified_gmt":"2024-02-05T19:42:27","slug":"specializovane-vysetreni-pro-dospele","status":"publish","type":"page","link":"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/","title":{"rendered":"Specialized examination for adults"},"content":{"rendered":"<div data-elementor-type=\"wp-page\" data-elementor-id=\"7396\" class=\"elementor elementor-7396\">\n\t\t\t\t<div class=\"elementor-element elementor-element-742fa1a e-flex e-con-boxed e-con e-parent\" data-id=\"742fa1a\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-ef930bd elementor-widget elementor-widget-spacer\" data-id=\"ef930bd\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-665cf25 e-flex e-con-boxed e-con e-parent\" data-id=\"665cf25\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-e046cc9 elementor-widget elementor-widget-text-editor\" data-id=\"e046cc9\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<h2>Ensure full examination package to your patients&nbsp;<\/h2>\n\n<p>We offer examinations that are covered by Genetika Plze\u0148.<\/p>\n\n<p>Types of examinations:<\/p>\n\n<ul><li><strong>Mutations of congenital thrombotic conditions<\/strong> \u2013 Leiden and prothrombin mutations. This examination is recommended for people who have suffered from thrombosis or embolism.<\/li><li><strong>Gilbert syndrome<\/strong> \u2013 molecular-genetic confirmation of benign hyperbilirubinemia.<\/li><li><strong>Haemochromatosis<\/strong> \u2013 the most common monogenic hereditary disorder leading to excessive iron accumulation in the hepatocytes and in the pancreas. The test is suitable for persons with elevated Fe, ALT, AST values, and with prolonged prothrombin time.<\/li><li><strong>Predisposition alleles for coeliac disease<\/strong> \u2013 individuals with reduced appetite, flatulence, constipation, anaemia, osteoporosis, increased tooth decay, joint pain, fatigue, infertility, and spontaneous abortions. If a patient has some of these symptoms and simultaneously carries predisposing alleles for celiac disease, it is recommended to follow a gluten-free diet.<\/li><li><strong>Lactose intolerance<\/strong> \u2013 intolerance to lactose afflicts about 10% of the Czech population, most often manifested by increased bloating, abdominal pain, or loose stools after consuming milk or dairy products containing lactose (milk sugar).<\/li><li><strong>Oncopanel of 22 genes analysed by NGS<\/strong> \u2013 these genes are mainly associated with the hereditary occurrence of breast, ovarian or colon cancers. This examination is suitable for individuals who had suffered from these diseases before the age of 50, or if they have a family history of one of these conditions in at least two generations in individuals under the age of 50.<\/li><li>We can refer patients for consultation in case of other&nbsp;<strong>monogenic hereditary disorders<\/strong>, that have already occurred in the family \u2013 primarily neurological diseases (Hereditary Motor-Sensory Neuropathy, Huntington's disease, spinocerebellar ataxia... ), kidney disorders (polycystic kidney disease, Alport syndrome...), cardiological diseases (Marfan syndrome and other connective tissue disorders, hereditary cardiomyopathies) or hearing disorders. In these cases, we perform a genetic consultation, informing the patient about the risk and significance of the test, and send the isolated DNA for testing to specialised laboratories in the Czech Republic or abroad.<\/li><li class=\" translation-block\"><strong>Examination of couples<\/strong> planning to conceive and having a congenital developmental defect or another hereditary disease. Following the genetic examination, the aim is to familiarize the couple with the genetic risk to their offspring and, alternatively, suggest eligible preventive measures (assisted reproduction with preimplantation genetic diagnostics and transfer of an embryo unaffected by the hereditary disorder).<\/li><\/ul>\n\n<p><strong>All of the above examinations are indicated by a clinical geneticist and are covered by Genetika Plze\u0148.<\/strong><\/p>\n\n<p class=\" translation-block\">Od&nbsp;v\u00e1s pacient pot\u0159ebuje doporu\u010den\u00ed ke genetick\u00e9mu vy\u0161et\u0159en\u00ed, kter\u00e9 je n\u00e1sledn\u011b mo\u017en\u00e9 objednat na&nbsp;telefonn\u00edch \u010d\u00edslech:&nbsp;<strong><a href=\"tel:+420377241529\" target=\"_self\">377&nbsp;241&nbsp;529<\/a><\/strong> nebo&nbsp;<strong><a href=\"tel:+420603174793\" target=\"_self\">603&nbsp;174&nbsp;793.<\/a><\/strong> N\u00e1sledn\u011b u&nbsp;n\u00e1s vyk\u00e1\u017eeme na&nbsp;va\u0161e pracovi\u0161t\u011b genetickou konzultaci za&nbsp;1522&nbsp;bod\u016f.<\/p>\n\n<p class=\" translation-block\">For patients covering care for themselves, our genetic consultation costs 1.500 CZK and following laboratory tests are charged at rates listed on our website www.genetika-plzen.cz.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-780ef4a e-flex e-con-boxed e-con e-parent\" data-id=\"780ef4a\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-2dbdec7 elementor-widget elementor-widget-image\" data-id=\"2dbdec7\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img fetchpriority=\"high\" decoding=\"async\" width=\"300\" height=\"284\" src=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_specializovane-vysetreni-pro-dospele-300x284.jpg\" class=\"attachment-medium size-medium wp-image-7398\" alt=\"\" srcset=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_specializovane-vysetreni-pro-dospele-300x284.jpg 300w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_specializovane-vysetreni-pro-dospele-768x727.jpg 768w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_specializovane-vysetreni-pro-dospele-13x12.jpg 13w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_specializovane-vysetreni-pro-dospele.jpg 837w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"<p>Zajist\u011bte sv\u00fdm pacient\u016fm plnohodnotn\u00e9 vy\u0161et\u0159en\u00ed&nbsp; Nab\u00edz\u00edme v\u00e1m vy\u0161et\u0159en\u00ed, kter\u00e1 jdou do&nbsp;n\u00e1klad\u016f Genetiky Plze\u0148. Druhy vy\u0161et\u0159en\u00ed: Mutace vrozeny\u0301ch tromboticky\u0301ch stav\u016f \u2013 Leidensk\u00e1 a&nbsp;protrombinov\u00e1 mutace. Toto vy\u0161et\u0159en\u00ed je vhodn\u00e9 doplnit u&nbsp;osob, kter\u00e9 prod\u011blaly tromb\u00f3zu \u010di&nbsp;embolii. Gilbert\u016fv syndrom \u2013 jedn\u00e1 se&nbsp;o&nbsp;molekul\u00e1rn\u011b genetick\u00e9 potvrzen\u00ed benign\u00ed hyperbilirubinemie. Hemochromatoza \u2013 nej\u010dast\u011bj\u0161\u00ed monogenn\u011b d\u011bdi\u010dn\u00e9 onemocn\u011bn\u00ed, kter\u00e9 vede k&nbsp;nadm\u011brn\u00e9mu st\u0159\u00e1d\u00e1n\u00ed \u017eeleza v&nbsp;hepatocytech a&nbsp;p\u0159edev\u0161\u00edm [&hellip;]<\/p>","protected":false},"author":9,"featured_media":0,"parent":7072,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"service-area":[27],"class_list":["post-7396","page","type-page","status-publish","hentry","service-area-geneticka-ambulance"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.2 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Specializovan\u00e9 vy\u0161et\u0159en\u00ed pro dosp\u011bl\u00e9 | Genetika Plze\u0148<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Specializovan\u00e9 vy\u0161et\u0159en\u00ed pro dosp\u011bl\u00e9 | Genetika Plze\u0148\" \/>\n<meta property=\"og:description\" content=\"Zajist\u011bte sv\u00fdm pacient\u016fm plnohodnotn\u00e9 vy\u0161et\u0159en\u00ed&nbsp; Nab\u00edz\u00edme v\u00e1m vy\u0161et\u0159en\u00ed, kter\u00e1 jdou do&nbsp;n\u00e1klad\u016f Genetiky Plze\u0148. Druhy vy\u0161et\u0159en\u00ed: Mutace vrozeny\u0301ch tromboticky\u0301ch stav\u016f \u2013 Leidensk\u00e1 a&nbsp;protrombinov\u00e1 mutace. Toto vy\u0161et\u0159en\u00ed je vhodn\u00e9 doplnit u&nbsp;osob, kter\u00e9 prod\u011blaly tromb\u00f3zu \u010di&nbsp;embolii. Gilbert\u016fv syndrom \u2013 jedn\u00e1 se&nbsp;o&nbsp;molekul\u00e1rn\u011b genetick\u00e9 potvrzen\u00ed benign\u00ed hyperbilirubinemie. Hemochromatoza \u2013 nej\u010dast\u011bj\u0161\u00ed monogenn\u011b d\u011bdi\u010dn\u00e9 onemocn\u011bn\u00ed, kter\u00e9 vede k&nbsp;nadm\u011brn\u00e9mu st\u0159\u00e1d\u00e1n\u00ed \u017eeleza v&nbsp;hepatocytech a&nbsp;p\u0159edev\u0161\u00edm [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/\" \/>\n<meta property=\"og:site_name\" content=\"Genetika Plze\u0148\" \/>\n<meta property=\"article:modified_time\" content=\"2024-02-05T19:42:27+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_specializovane-vysetreni-pro-dospele-300x284.jpg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Estimated reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/de\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/\",\"url\":\"https:\/\/genetika-plzen.nullable.group\/de\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/\",\"name\":\"Specializovan\u00e9 vy\u0161et\u0159en\u00ed pro dosp\u011bl\u00e9 | Genetika Plze\u0148\",\"isPartOf\":{\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#website\"},\"datePublished\":\"2024-02-05T19:39:18+00:00\",\"dateModified\":\"2024-02-05T19:42:27+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/genetika-plzen.nullable.group\/de\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/#breadcrumb\"},\"inLanguage\":\"en-GB\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/genetika-plzen.nullable.group\/de\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/de\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/genetika-plzen.nullable.group\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Genetick\u00e1 ambulance\",\"item\":\"https:\/\/genetika-plzen.nullable.group\/de\/geneticka-ambulance\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Specializovan\u00e9 vy\u0161et\u0159en\u00ed pro dosp\u011bl\u00e9\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#website\",\"url\":\"https:\/\/genetika-plzen.nullable.group\/\",\"name\":\"Genetika Plze\u0148\",\"description\":\"Genetika Plze\u0148\",\"publisher\":{\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/genetika-plzen.nullable.group\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"en-GB\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#organization\",\"name\":\"Genetika Plze\u0148\",\"url\":\"https:\/\/genetika-plzen.nullable.group\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-GB\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#\/schema\/logo\/image\/\",\"url\":\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2022\/07\/logo2.svg\",\"contentUrl\":\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2022\/07\/logo2.svg\",\"width\":286,\"height\":95,\"caption\":\"Genetika Plze\u0148\"},\"image\":{\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#\/schema\/logo\/image\/\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Specializovan\u00e9 vy\u0161et\u0159en\u00ed pro dosp\u011bl\u00e9 | Genetika Plze\u0148","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/specializovane-vysetreni-pro-dospele\/","og_locale":"en_GB","og_type":"article","og_title":"Specializovan\u00e9 vy\u0161et\u0159en\u00ed pro dosp\u011bl\u00e9 | Genetika Plze\u0148","og_description":"Zajist\u011bte sv\u00fdm pacient\u016fm plnohodnotn\u00e9 vy\u0161et\u0159en\u00ed&nbsp; Nab\u00edz\u00edme v\u00e1m vy\u0161et\u0159en\u00ed, kter\u00e1 jdou do&nbsp;n\u00e1klad\u016f Genetiky Plze\u0148. Druhy vy\u0161et\u0159en\u00ed: Mutace vrozeny\u0301ch tromboticky\u0301ch stav\u016f \u2013 Leidensk\u00e1 a&nbsp;protrombinov\u00e1 mutace. Toto vy\u0161et\u0159en\u00ed je vhodn\u00e9 doplnit u&nbsp;osob, kter\u00e9 prod\u011blaly tromb\u00f3zu \u010di&nbsp;embolii. Gilbert\u016fv syndrom \u2013 jedn\u00e1 se&nbsp;o&nbsp;molekul\u00e1rn\u011b genetick\u00e9 potvrzen\u00ed benign\u00ed hyperbilirubinemie. 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