{"id":7402,"date":"2024-02-05T20:40:25","date_gmt":"2024-02-05T19:40:25","guid":{"rendered":"https:\/\/genetika-plzen.nullable.group\/?page_id=7402"},"modified":"2024-06-08T11:26:41","modified_gmt":"2024-06-08T09:26:41","slug":"vysetreni-pro-detske-pacienty","status":"publish","type":"page","link":"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/","title":{"rendered":"Examinations for infants and children"},"content":{"rendered":"<div data-elementor-type=\"wp-page\" data-elementor-id=\"7402\" class=\"elementor elementor-7402\">\n\t\t\t\t<div class=\"elementor-element elementor-element-62f9a62 e-flex e-con-boxed e-con e-parent\" data-id=\"62f9a62\" 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-081a57c elementor-widget elementor-widget-spacer\" data-id=\"081a57c\" 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-d21f64d e-flex e-con-boxed e-con e-parent\" data-id=\"d21f64d\" 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-ab48824 elementor-widget elementor-widget-text-editor\" data-id=\"ab48824\" 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 infant patients.<\/h2>\n\n<p>We offer examinations that are covered by Genetika Plze\u0148.<\/p>\n\n<ul><li><strong>Examination of the karyotype or exclusion of the most frequent microdeletion and microduplication syndromes using the array CGH method<\/strong>\n \u2013 starting from newborns, toddlers, and infants with signs of facial dysmorphism, congenital developmental defects, growth and behavioural disorders, hypotonia, or autism spectrum disorders (ASD). For karyotyping, we routinely perform blood draw, examination using array CGH may also be performed non-invasively from the buccal swab.<\/li><li><strong>Predisposition alleles for coeliac disease <\/strong>\u2013 infants with reduced appetite, failing to thrive, bloating, constipation, anaemia, osteoporosis, increased tooth decay, joint pain, fatigue, growth disorders, atopic dermatitis, and recurrent respiratory infections. Suitable for parents who reject enterobiopsy (the molecular-genetic test can be performed non-invasively from the buccal swab). <strong>The genetic examination neither confirms nor excludes the celiac disease diagnosis, it only determines genetic predispositions.<\/strong><\/li><li><strong>Lactose intolerance<\/strong> \u2013 nesn\u00e1\u0161enlivost lakt\u00f3zy tr\u00e1p\u00ed\n zhruba 10&nbsp;% obyvatel \u010cesk\u00e9 republiky \u2013 nej\u010dast\u011bji se&nbsp;projevuje \nzvy\u0301\u0161eny\u0301m nady\u0301m\u00e1n\u00edm, bolestmi b\u0159icha nebo&nbsp;\u0159\u00eddky\u0301mi stolicemi \npo&nbsp;konzumaci ml\u00e9ka \u010di&nbsp;ml\u00e9\u010dny\u0301ch vy\u0301robk\u016f, kter\u00e9 obsahuj\u00ed lakt\u00f3zu \n(ml\u00e9\u010dny\u0301 cukr).<\/li><li><strong>Mutations of congenital thrombotic conditions<\/strong> \u2013 Leiden and prothrombin mutations. This examination is recommended for children (particularly adolescent girls), whose relatives have either suffered from thrombosis \/ embolism or carry a thrombophilic mutation. The test ca be performed non-invasively from the buccal swab.<\/li><li><strong>Gilbert syndrome<\/strong> \u2013 molecular-genetic confirmation of benign hyperbilirubinemia. The test ca be performed non-invasively from the buccal swab.<\/li><li class=\" translation-block\">We can refer patients for consultation in case of other monogenic hereditary disorders 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. The examination usually requires a blood draw.<\/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><u><strong>Your patient will require<\/strong><\/u><br>\n<strong>a requisition form for the genetic examination<\/strong>, which is available by ordering on phone numbers&nbsp;<strong><a href=\"tel: 420377241529\">377&nbsp;241&nbsp;529<\/a><\/strong> or&nbsp;<strong><a href=\"tel: 420603174793\">603&nbsp;174&nbsp;793<\/a><\/strong>. For examinations of children below 18 years of age, the informed consent of a legal representative is required (signed on site). Please instruct parents to bring a report from the maternity hospital, their child's vaccination certificate, and copies of the results of specialist examinations, if applicable.<\/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-f88c66a elementor-widget elementor-widget-button\" data-id=\"f88c66a\" 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\/03\/med_2023_letak_genetika_pediatr_A5_04_tisk.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\">Leaflet<\/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-9117dd8 elementor-widget elementor-widget-button\" data-id=\"9117dd8\" 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-size-sm\" role=\"button\">\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 legal guardian for a minor patient older than 15 years<\/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-65a9745 elementor-widget elementor-widget-button\" data-id=\"65a9745\" 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 to genetic laboratory 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-8c522fd elementor-widget elementor-widget-button\" data-id=\"8c522fd\" 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\">Guide to cytogenetic examination<\/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-0c91780 elementor-widget elementor-widget-button\" data-id=\"0c91780\" 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-69ed925 e-flex e-con-boxed e-con e-parent\" data-id=\"69ed925\" 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-7529338 elementor-widget elementor-widget-image\" data-id=\"7529338\" 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=\"283\" src=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_vysetreni-pro-detske-pacienty-300x283.jpg\" class=\"attachment-medium size-medium wp-image-7404\" alt=\"\" srcset=\"https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_vysetreni-pro-detske-pacienty-300x283.jpg 300w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_vysetreni-pro-detske-pacienty-768x726.jpg 768w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_vysetreni-pro-detske-pacienty-13x12.jpg 13w, https:\/\/genetika-plzen.nullable.group\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_vysetreni-pro-detske-pacienty.jpg 836w\" 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<div class=\"elementor-element elementor-element-adbfc16 elementor-widget elementor-widget-spacer\" data-id=\"adbfc16\" 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>Zajist\u011bte svy\u0301m d\u011btsky\u0301m pacient\u016fm plnohodnotn\u00e9 vy\u0161et\u0159en\u00ed. Nab\u00edz\u00edme v\u00e1m vy\u0161et\u0159en\u00ed, kter\u00e1 jdou do&nbsp;n\u00e1klad\u016f Genetiky Plze\u0148. Vy\u0161et\u0159en\u00ed karyotypu, pop\u0159. vylou\u010den\u00ed nej\u010dast\u011bj\u0161\u00edch mikrodele\u010dn\u00edch a&nbsp;mikroduplika\u010dn\u00edch syndrom\u016f metodou array CGH \u2013 ji\u017e u&nbsp;novorozenc\u016f, kojenc\u016f a&nbsp;maly\u0301ch d\u011bt\u00ed se&nbsp;zn\u00e1mkami faci\u00e1ln\u00ed dysmorfie, vrozeny\u0301mi vy\u0301vojovy\u0301mi vadami, poruchami r\u016fstu, hypotoni\u00ed, poruchami chov\u00e1n\u00ed, PAS&nbsp;Pro&nbsp;stanoven\u00ed karyotypu prov\u00e1d\u00edme obvykle venosn\u00ed odb\u011br, vy\u0161et\u0159en\u00ed metodou array \u2013 CGH lze v&nbsp;indikovany\u0301ch [&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-7402","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>Vy\u0161et\u0159en\u00ed pro d\u011btsk\u00e9 pacienty | 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\/vysetreni-pro-detske-pacienty\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Vy\u0161et\u0159en\u00ed pro d\u011btsk\u00e9 pacienty | Genetika Plze\u0148\" \/>\n<meta property=\"og:description\" content=\"Zajist\u011bte svy\u0301m d\u011btsky\u0301m pacient\u016fm plnohodnotn\u00e9 vy\u0161et\u0159en\u00ed. Nab\u00edz\u00edme v\u00e1m vy\u0161et\u0159en\u00ed, kter\u00e1 jdou do&nbsp;n\u00e1klad\u016f Genetiky Plze\u0148. Vy\u0161et\u0159en\u00ed karyotypu, pop\u0159. vylou\u010den\u00ed nej\u010dast\u011bj\u0161\u00edch mikrodele\u010dn\u00edch a&nbsp;mikroduplika\u010dn\u00edch syndrom\u016f metodou array CGH \u2013 ji\u017e u&nbsp;novorozenc\u016f, kojenc\u016f a&nbsp;maly\u0301ch d\u011bt\u00ed se&nbsp;zn\u00e1mkami faci\u00e1ln\u00ed dysmorfie, vrozeny\u0301mi vy\u0301vojovy\u0301mi vadami, poruchami r\u016fstu, hypotoni\u00ed, poruchami chov\u00e1n\u00ed, PAS&nbsp;Pro&nbsp;stanoven\u00ed karyotypu prov\u00e1d\u00edme obvykle venosn\u00ed odb\u011br, vy\u0161et\u0159en\u00ed metodou array \u2013 CGH lze v&nbsp;indikovany\u0301ch [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/genetika-plzen.nullable.group\/en\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/\" \/>\n<meta property=\"og:site_name\" content=\"Genetika Plze\u0148\" \/>\n<meta property=\"article:modified_time\" content=\"2024-06-08T09:26:41+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.genetika-plzen.cz\/wp-content\/uploads\/2024\/02\/thumb_3000x3000_vysetreni-pro-detske-pacienty-300x283.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=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/\",\"url\":\"https:\/\/genetika-plzen.nullable.group\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/\",\"name\":\"Vy\u0161et\u0159en\u00ed pro d\u011btsk\u00e9 pacienty | Genetika Plze\u0148\",\"isPartOf\":{\"@id\":\"https:\/\/genetika-plzen.nullable.group\/#website\"},\"datePublished\":\"2024-02-05T19:40:25+00:00\",\"dateModified\":\"2024-06-08T09:26:41+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/genetika-plzen.nullable.group\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/#breadcrumb\"},\"inLanguage\":\"en-GB\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/genetika-plzen.nullable.group\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/genetika-plzen.nullable.group\/geneticka-ambulance\/vysetreni-pro-detske-pacienty\/#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\":\"Vy\u0161et\u0159en\u00ed pro d\u011btsk\u00e9 pacienty\"}]},{\"@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":"Vy\u0161et\u0159en\u00ed pro d\u011btsk\u00e9 pacienty | 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\/vysetreni-pro-detske-pacienty\/","og_locale":"en_GB","og_type":"article","og_title":"Vy\u0161et\u0159en\u00ed pro d\u011btsk\u00e9 pacienty | Genetika Plze\u0148","og_description":"Zajist\u011bte svy\u0301m d\u011btsky\u0301m pacient\u016fm plnohodnotn\u00e9 vy\u0161et\u0159en\u00ed. 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