{"id":7094,"date":"2022-01-05T16:02:31","date_gmt":"2022-01-05T16:02:31","guid":{"rendered":"http:\/\/localhost\/bhc-dev\/?page_id=7094"},"modified":"2022-01-07T11:28:21","modified_gmt":"2022-01-07T11:28:21","slug":"komplettes-screening-panel","status":"publish","type":"page","link":"https:\/\/www.babyhealthcheck.com\/at\/komplettes-screening-panel\/","title":{"rendered":"Komplettes Screening-Panel"},"content":{"rendered":"\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\" style=\"flex-basis:80%\">\n<h2 class=\"py-3 mb-3\">Das&nbsp;<span style=\"color:#7b67ab\" class=\"has-inline-color\">Baby Health Check<\/span>&nbsp;Programm bietet eine umfassende Analyse sowie die zus\u00e4tzliche Flexibilit\u00e4t, Ihr Screening-Panel zu personalisieren.<\/h2>\n\n\n\n<h3 class=\"py-3\">Was sind Ihre Vorteile eines&nbsp;<span style=\"color:#7b67ab\" class=\"has-inline-color\">personalisierten Screening-Panels?<\/span><\/h3>\n\n\n\n<ul class=\"pink-checks\"><li>Zugang zur Untersuchung von weiteren wichtigen Erkrankungen \u2013 zus\u00e4tzlich zu jenen, die von staatlichen Screening-Programmen angeboten werden<\/li><li>Schnellere Identifizierung von Krankheiten in schwierigen F\u00e4llen (z. B. bei bekannter famili\u00e4rer Vorbelastung angeborener Erkrankungen)<\/li><li>Ein Expertenteam, das Sie und Ihre Patienten bei der komplexen Diagnostik unterst\u00fctzt<\/li><li>Die einzigartige Gelegenheit, zu Initiativen des Neugeborenen-Screenings beizutragen, um somit die Testung f\u00fcr weitere behandelbare Seltene Erkrankungen zu erweitern<\/li><\/ul>\n\n\n\n<div class=\"wp-container-1 wp-block-buttons\">\n<div class=\"wp-block-button has-custom-font-size my-5 has-normal-font-size\"><a class=\"wp-block-button__link has-white-color has-text-color has-background no-border-radius\" href=\"mailto:info@archimedlife.com?subject=BHC Screening Panel\" style=\"background-color:#7b67ab\">Kontaktieren Sie uns<br>um Ihr personalisiertes Screening-Panel zu besprechen<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column pt-3\" style=\"flex-basis:80%\">\n<p style=\"font-size:18px\"><strong><strong>Finden Sie hier das komplette Screening-Panel mit \u00fcber 70 Seltenen Erkrankungen<\/strong><\/strong><\/p>\n\n\n\n<section class=\"wp-container-2 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Aminoazid\u00e4mie<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Arginin\u00e4mie<br>Argininsuccins\u00e4ure-Syndrom<br>Citrullinan\u00e4mie, Typ I<br>Citrullin\u00e4mie, Typ II<br>Phenylketonurie<br>Homocystinurie<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Hypermethionin\u00e4mie<br>Hyperphenylalanin\u00e4mie<br>Ahornsiruperkrankung<br>Tyrosin\u00e4mie, Typ I (Succinylaceton; SUAC)<br>Tyrosin\u00e4mie, Typ II<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-3 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Carnitin- und Fettstoffwechseldefekt<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Carnitin-Transporter Mangel<br>Medium-chain Acyl-CoA Dehydrogenase Mangel<br>Very long-chain Acyl-CoA Dehydrogenase Mangel<br>Long-chain L-3 hydroxyacyl-CoA Dehydrogenase Mangel<br>Mitochondriale trifunktionale Protein (MTP, TFP) Mangel<br>Short-chain acyl-CoA Dehydrogenase Mangel<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Medium\/short-chain L-3-hydroxyacyl-CoA Dehydrogenase Mangel<br>Medium-chain Ketoacyl-CoA-Thiolase Mangel<br>2,4 Dienoyl-CoA-Reduktase-Mangel<br>Carnitin-Palmitoyl-Transferase I Mangel<br>Carnitin-Palmitoyl-Transferase II Mangel<br>Carnitin-Acylcarnitin-Translokase Mangel (CACT)<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-4 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Organazidurie<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Propions\u00e4urean\u00e4mie<br>Methylmalons\u00e4urean\u00e4mie (Methylmalonyl-CoA-Mutase)<br>Methylmalons\u00e4urean\u00e4mie (Cobalaminst\u00f6rungen)<br>Isovalerians\u00e4ure-An\u00e4mie<br>3-Methylcrotonyl-CoA-Carboxylase-Mangel<br>3-Hydroxy-3-methylglutars\u00e4ureurie<br>Holocarboxylase-Synthetase-Mangel<br>\u00df-Ketothiolase-Mangel<br>Glutars\u00e4urean\u00e4mie Typ I<br>Glutars\u00e4urean\u00e4mie Typ II<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Methylmalons\u00e4urean\u00e4mie mit Homocystinurie<br>Malons\u00e4urean\u00e4mie<br>Isobutyryl-CoA-Dehydrogenase-Mangel<br>2-Methylbutyryl-CoA-Dehydrogenase-Mangel<br>3-Methylglutacons\u00e4ureurie Typ I<br>2-Methyl-3-Hydroxybutters\u00e4ure-Syndrom<br>3-Methylglutacons\u00e4ureurie Typ II, III, IV, V<br>Kombinierte Malon- und Methylmalons\u00e4ureurie<br>Ornithin-Transcarbamylase-Mangel<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-5 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Lysosomale Speicherkrankheiten (LSD)<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Morbus Fabry<br>Morbus Gaucher<br>Morbus Pompe<br>Morbus Krabbe<br>Morbus Niemann-Pick A \/ B<br>Mukopolysaccharidose I<br>Mukopolysaccharidose II<br>Mukopolysaccharidose IIIB<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Mukopolysaccharidose IVA<br>Mukopolysaccharidose IVB<br>Mukopolysaccharidose VI<br>Mukopolysaccharidose VII<br>\u03b1-Mannosidase<br>Neuronale Ceroid-Lipofuszinose 1<br>Neuronale Ceroid-Lipofuszinose 2<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-6 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Schwere kombinierte Immundefizienz (SCID)<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>TREC- und KREC-Tests f\u00fcr T- und B-Zell-Immundefizienz<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Adenosin-Desaminase Mangel (ADA-Mangel)<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-7 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Endokrine St\u00f6rung<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Kongenitale Hypothyreose<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Adrenogenitales Syndrom<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-8 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>Neuromuskul\u00e4re und peroxisomale St\u00f6rungen<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>5q-Spinale Muskelatrophie<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>X-chromosomale Adrenoleukodystrophie<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<section class=\"wp-container-9 wp-block-group disease-block\"><div class=\"wp-block-group__inner-container\">\n<h4>weitere Erkrankungen<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Biotinidase-Mangel<br>Galaktos\u00e4mie (Galaktos\u00e4mie Typ I)<br>Glucose-6-phosphat-Dehydrogenase-Mangel<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Zystische Fibrose<br>Sichelzellenan\u00e4mie<br>Cerebrotendin\u00f6se Xanthomatose (CTX)<\/p>\n<\/div>\n<\/div>\n<\/div><\/section>\n\n\n\n<div class=\"wp-container-10 wp-block-buttons\">\n<div class=\"wp-block-button has-custom-font-size my-5 has-normal-font-size\"><a class=\"wp-block-button__link has-white-color has-text-color has-background no-border-radius\" href=\"mailto:info@archimedlife.com?subject=BHC Screening Panel\" style=\"background-color:#7b67ab\">Kontaktieren Sie uns<br>um Ihr personalisiertes Screening-Panel zu besprechen<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Das&nbsp;Baby Health Check&nbsp;Programm bietet eine umfassende Analyse sowie die zus\u00e4tzliche Flexibilit\u00e4t, Ihr Screening-Panel zu personalisieren. Was sind Ihre Vorteile eines&nbsp;personalisierten Screening-Panels? Zugang zur Untersuchung von weiteren wichtigen Erkrankungen \u2013 zus\u00e4tzlich zu jenen, die von staatlichen Screening-Programmen angeboten werden Schnellere Identifizierung von Krankheiten in schwierigen F\u00e4llen (z. B. bei bekannter famili\u00e4rer Vorbelastung angeborener Erkrankungen) Ein Expertenteam,<\/p>\n","protected":false},"author":1,"featured_media":4648,"parent":0,"menu_order":5,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"acf":[],"uagb_featured_image_src":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false},"uagb_author_info":{"display_name":"admin","author_link":"https:\/\/www.babyhealthcheck.com\/at\/author\/admin\/"},"uagb_comment_info":0,"uagb_excerpt":"Das&nbsp;Baby Health Check&nbsp;Programm bietet eine umfassende Analyse sowie die zus\u00e4tzliche Flexibilit\u00e4t, Ihr Screening-Panel zu personalisieren. Was sind Ihre Vorteile eines&nbsp;personalisierten Screening-Panels? Zugang zur Untersuchung von weiteren wichtigen Erkrankungen \u2013 zus\u00e4tzlich zu jenen, die von staatlichen Screening-Programmen angeboten werden Schnellere Identifizierung von Krankheiten in schwierigen F\u00e4llen (z. B. bei bekannter famili\u00e4rer Vorbelastung angeborener Erkrankungen) Ein Expertenteam,","_links":{"self":[{"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages\/7094"}],"collection":[{"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/comments?post=7094"}],"version-history":[{"count":2,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages\/7094\/revisions"}],"predecessor-version":[{"id":7228,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages\/7094\/revisions\/7228"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/"}],"wp:attachment":[{"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/media?parent=7094"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}