{"id":7175,"date":"2024-02-04T00:20:29","date_gmt":"2024-02-03T23:20:29","guid":{"rendered":"https:\/\/genetika-plzen.nullable.group\/?page_id=7175"},"modified":"2024-06-08T11:23:31","modified_gmt":"2024-06-08T09:23:31","slug":"lekarska-genetika-geneticke-vysetreni","status":"publish","type":"page","link":"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/lekarska-genetika-geneticke-vysetreni\/","title":{"rendered":"Medical genetics"},"content":{"rendered":"<div data-elementor-type=\"wp-page\" data-elementor-id=\"7175\" class=\"elementor elementor-7175\">\n\t\t\t\t<div class=\"elementor-element elementor-element-95a60b3 e-flex e-con-boxed e-con e-parent\" data-id=\"95a60b3\" 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-ee0bac5 elementor-widget elementor-widget-spacer\" data-id=\"ee0bac5\" 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-eabb699 e-flex e-con-boxed e-con e-parent\" data-id=\"eabb699\" 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-20ecb28 elementor-widget elementor-widget-text-editor\" data-id=\"20ecb28\" 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\tGenetic examination consists of a genetic consultation with the creation of a pedigree for the client or both partners \u2013 information about siblings, parents, aunts and uncles, and grandparents. In the family, we are particularly interested in congenital developmental defects (cleft lip, palate, heart defects\u2026), mental retardation, serious diseases (heart attacks, strokes, malignant tumors), and possibly causes of death. After creating the pedigree, we compile a personal medical history \u2013 in the case of long-term treatment, it is advisable to supplement this information with medical documentation. A blood sample is often part of the genetic consultation, along with an introduction to the examinations we will conduct.\n<h2>TYPES OF EXAMINATIONS:<\/h2>\n<ol type=\"a\">\n \t<li>GENETIC EXAMINATION FOR COUPLES WITH FERTILITY DISORDERS\n<ul>\n \t<li><a href=\"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/prekoncepcni-geneticke-vysetreni-carrier-screening\/\">Preconception genetic testing<\/a><\/li>\n \t<li><a href=\"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/carrier-screening\/\">Carrier screening<\/a><\/li>\n<\/ul>\n<\/li>\n \t<li><a href=\"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/\">GENETIC EXAMINATION OF CHILDREN WITH CONGENITAL DEFECTS<\/a><\/li>\n \t<li>GENETIC EXAMINATION FOR PATIENTS AT RISK OF SERIOUS DISEASES\n<\/li>\n<\/ul>\n<\/li>\n<\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-fed020c elementor-widget elementor-widget-accordion\" data-id=\"fed020c\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"accordion.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-accordion\">\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2671\" class=\"elementor-tab-title\" data-tab=\"1\" role=\"button\" aria-controls=\"elementor-tab-content-2671\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Oncopanel Examination<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2671\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"1\" role=\"region\" aria-labelledby=\"elementor-tab-title-2671\"><p>These are genes primarily associated with the hereditary occurrence of breast, ovarian, and colon cancers. This examination is suitable for individuals who have experienced any of these diseases before the age of 50, or if there is a family history of any of these diseases in at least two generations in individuals under 50 years of age.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2672\" class=\"elementor-tab-title\" data-tab=\"2\" role=\"button\" aria-controls=\"elementor-tab-content-2672\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Mutations of Congenital Thrombotic Conditions<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2672\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"2\" role=\"region\" aria-labelledby=\"elementor-tab-title-2672\"><p>Leiden and Prothrombin Mutations. This examination is advisable for individuals who have experienced thrombosis or embolism.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2673\" class=\"elementor-tab-title\" data-tab=\"3\" role=\"button\" aria-controls=\"elementor-tab-content-2673\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Gilbert syndrome<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2673\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"3\" role=\"region\" aria-labelledby=\"elementor-tab-title-2673\"><p>It involves molecular genetic confirmation of benign hyperbilirubinemia.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2674\" class=\"elementor-tab-title\" data-tab=\"4\" role=\"button\" aria-controls=\"elementor-tab-content-2674\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Haemochromatosis<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2674\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"4\" role=\"region\" aria-labelledby=\"elementor-tab-title-2674\"><p>The most common monogenic hereditary disease leads to excessive iron accumulation in hepatocytes and especially the pancreas. It is suitable to complement in individuals with elevated Fe, ALT, AST levels, with prolonged prothrombin time.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2675\" class=\"elementor-tab-title\" data-tab=\"5\" role=\"button\" aria-controls=\"elementor-tab-content-2675\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Predisposing alleles for celiac disease<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2675\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"5\" role=\"region\" aria-labelledby=\"elementor-tab-title-2675\"><p>In individuals with reduced appetite, bloating, constipation, anemia, osteoporosis, increased tooth decay, joint pain, fatigue, and infertility, spontaneous miscarriages. If a patient has some of these issues and simultaneously has predispositions for celiac disease, it is advisable to start adhering to a gluten-free diet.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2676\" class=\"elementor-tab-title\" data-tab=\"6\" role=\"button\" aria-controls=\"elementor-tab-content-2676\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Lactose intolerance<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2676\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"6\" role=\"region\" aria-labelledby=\"elementor-tab-title-2676\"><p>Affects about 10% of the Czech Republic's population \u2013 it most often manifests as increased bloating, abdominal pain, or loose stools after consuming milk or dairy products that contain lactose (milk sugar).<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<div class=\"elementor-accordion-item\">\n\t\t\t\t\t<div id=\"elementor-tab-title-2677\" class=\"elementor-tab-title\" data-tab=\"7\" role=\"button\" aria-controls=\"elementor-tab-content-2677\" aria-expanded=\"false\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon elementor-accordion-icon-left\" aria-hidden=\"true\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-closed\"><i class=\"fas fa-plus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t<span class=\"elementor-accordion-icon-opened\"><i class=\"fas fa-minus\"><\/i><\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t<a class=\"elementor-accordion-title\" tabindex=\"0\">Other monogenic hereditary diseases<\/a>\n\t\t\t\t\t<\/div>\n\t\t\t\t\t<div id=\"elementor-tab-content-2677\" class=\"elementor-tab-content elementor-clearfix\" data-tab=\"7\" role=\"region\" aria-labelledby=\"elementor-tab-title-2677\"><p>Other monogenic hereditary diseases primarily include:<\/p><ul><li>Neurological diseases \u2013 Huntington's disease, spinocerebellar ataxia\u2026<\/li><li>Kidney diseases \u2013 Polycystic kidney disease, Alport syndrome\u2026<\/li><li>Cardiological diseases \u2013 Marfan syndrome and other connective tissue disorders, hereditary cardiomyopathies<\/li><li>Hearing disorders \u2013 Connexin 26 examination (mutations 35delG, W24X)<\/li><\/ul><p>\u00a0<\/p><p>In these cases, we conduct a genetic consultation, educate the patient about the risk and significance of the examination for them, and send isolated DNA for examination to specialized laboratories in the Czech Republic or abroad.<\/p><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-caec4f0 elementor-widget elementor-widget-text-editor\" data-id=\"caec4f0\" 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<p align=\"left\"><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"><b>All mentioned examinations are indicated by a clinical geneticist and requested by our facility. They are thus included in the costs of Genetics Plze\u0148.<\/b><\/span><\/span><\/span><\/span><\/p><p align=\"left\"><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\">From you, the patient needs a referral for genetic examination, which can then be ordered at the phone numbers: <\/span><\/span><\/span><\/span><span style=\"color: #0563c1;\"><a href=\"tel: 420377241529\"><span style=\"color: #cc3366;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"><b>377 241 529<\/b><\/span><\/span><\/span><\/span><\/a><\/span><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"> or <\/span><\/span><\/span><\/span><span style=\"color: #0563c1;\"><a href=\"tel: 420603174793\"><span style=\"color: #cc3366;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"><b>603 174 793.<\/b><\/span><\/span><\/span><\/span><\/a><\/span><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"> Subsequently, we will report the genetic consultation to your facility for 1522 points.<\/span><\/span><\/span><\/span><\/p><p align=\"left\"><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\">For self-paying patients, <\/span><\/span><\/span><\/span><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"><b>the genetic consultation with us is 1,500 CZK<\/b><\/span><\/span><\/span><\/span><span style=\"color: #7a7a7a;\"><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"> , and other laboratory tests are charged at the price you can find on our website <\/span><\/span><\/span><\/span><span style=\"color: #0563c1;\"><u><span style=\"font-family: Roboto, serif;\"><span style=\"font-size: medium;\"><span lang=\"cs-CZ\"><b>www.genetika-plzen.cz<\/b><\/span><\/span><\/span><\/u><\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ed1c55a elementor-button-info elementor-widget elementor-widget-button\" data-id=\"ed1c55a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"button.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<div class=\"elementor-button-wrapper\">\n\t\t\t\t\t<a class=\"elementor-button elementor-button-link elementor-size-sm\" href=\"\/wp-content\/uploads\/2024\/06\/F.GP-901-v002-EN-Consent-with-genetic-laboratory__-examination_interactive.pdf\">\n\t\t\t\t\t\t<span class=\"elementor-button-content-wrapper\">\n\t\t\t\t\t\t\t\t\t<span class=\"elementor-button-text\">Consent of the subject<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-12b9db0 elementor-button-info elementor-widget elementor-widget-button\" data-id=\"12b9db0\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"button.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<div class=\"elementor-button-wrapper\">\n\t\t\t\t\t<a class=\"elementor-button elementor-button-link elementor-size-sm\" href=\"\/wp-content\/uploads\/2024\/06\/F.GP-910-v003-EN-Requisition-for-cytogenetic-test_interactive.pdf\">\n\t\t\t\t\t\t<span class=\"elementor-button-content-wrapper\">\n\t\t\t\t\t\t\t\t\t<span class=\"elementor-button-text\">Referral for cytogenetic testing<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-c0d63cf elementor-button-info elementor-widget elementor-widget-button\" data-id=\"c0d63cf\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"button.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<div class=\"elementor-button-wrapper\">\n\t\t\t\t\t<a class=\"elementor-button elementor-button-link elementor-size-sm\" href=\"\/wp-content\/uploads\/2024\/06\/F.GP-911-v003-EN-Requisition-for-molecular-genetics-test_interactive.pdf\">\n\t\t\t\t\t\t<span class=\"elementor-button-content-wrapper\">\n\t\t\t\t\t\t\t\t\t<span class=\"elementor-button-text\">Guide to molecular genetic testing<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t<\/div>\n\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-319d694 e-flex e-con-boxed e-con e-parent\" data-id=\"319d694\" 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-7fbce83 elementor-widget elementor-widget-image\" data-id=\"7fbce83\" 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=\"500\" height=\"500\" src=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_lekarska-genetika-geneticke-vysetreni.jpg\" class=\"attachment-large size-large wp-image-7177\" alt=\"\" srcset=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_lekarska-genetika-geneticke-vysetreni.jpg 500w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_lekarska-genetika-geneticke-vysetreni-300x300.jpg 300w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_lekarska-genetika-geneticke-vysetreni-150x150.jpg 150w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/>\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<div class=\"elementor-element elementor-element-007243b e-flex e-con-boxed e-con e-parent\" data-id=\"007243b\" 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-f9c0257 elementor-widget elementor-widget-spacer\" data-id=\"f9c0257\" 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\t\t<\/div>","protected":false},"excerpt":{"rendered":"<p>Genetick\u00e9 vy\u0161et\u0159en\u00ed sest\u00e1v\u00e1 z\u00a0genetick\u00e9 konzultace s\u00a0vytvo\u0159en\u00edm rodokmenu klienta nebo\u00a0obou partner\u016f &#8211; informace o\u00a0sourozenc\u00edch, rodi\u010d\u00edch, tet\u00e1ch a\u00a0str\u00fdc\u00edch a\u00a0prarodi\u010d\u00edch. V\u00a0rodin\u011b n\u00e1s zaj\u00edmaj\u00ed p\u0159edev\u0161\u00edm vrozen\u00e9 v\u00fdvojov\u00e9 vady (roz\u0161t\u011bpy rtu, patra, srde\u010dn\u00ed vady.\u2026.), ment\u00e1ln\u00ed retardace, z\u00e1va\u017en\u00e1 onemocn\u011bn\u00ed (infarkty, mrtvice, zhoubn\u00e9 n\u00e1dory) event. p\u0159\u00ed\u010diny \u00famrt\u00ed. Po\u00a0vytvo\u0159en\u00ed rodokmenu sestavujeme osobn\u00ed zdravotn\u00ed anamn\u00e9zu \u2013 v\u00a0p\u0159\u00edpad\u011b dlouhodob\u00e9 l\u00e9\u010dby je vhodn\u00e9 doplnit tyto informace [&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-7175","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>L\u00e9ka\u0159sk\u00e1 genetika | 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\/lekarska-genetika-geneticke-vysetreni\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"L\u00e9ka\u0159sk\u00e1 genetika | Genetika Plze\u0148\" \/>\n<meta property=\"og:description\" content=\"Genetick\u00e9 vy\u0161et\u0159en\u00ed sest\u00e1v\u00e1 z\u00a0genetick\u00e9 konzultace s\u00a0vytvo\u0159en\u00edm rodokmenu klienta nebo\u00a0obou partner\u016f &#8211; informace o\u00a0sourozenc\u00edch, rodi\u010d\u00edch, tet\u00e1ch a\u00a0str\u00fdc\u00edch a\u00a0prarodi\u010d\u00edch. 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