{"id":6729,"date":"2021-12-21T15:21:57","date_gmt":"2021-12-21T15:21:57","guid":{"rendered":"https:\/\/www.babyhealthcheck.com\/?page_id=6729"},"modified":"2022-01-26T09:46:15","modified_gmt":"2022-01-26T09:46:15","slug":"complete-newborn-screening-panel","status":"publish","type":"page","link":"https:\/\/www.babyhealthcheck.com\/at\/complete-newborn-screening-panel\/?lang=en","title":{"rendered":"Complete 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\">The&nbsp;Baby Health Check&nbsp;screening program delivers comprehensive analysis with the flexibility to personalize your screening program.<\/h2>\n\n\n\n<h3 class=\"py-3\">What are Your Benefits of a Personalized Screening Panel?<\/h3>\n\n\n\n<ul class=\"pink-checks\"><li>Access to Newborn Screening for more diseases in addition to those which may be provided by local screening programs<\/li><li>Faster disease identification in difficult cases (e.g. known family history of disease)<\/li><li>An expert team supporting you and your patients through sometimes complex diagnostics<\/li><li>A unique opportunity to contribute to newborn screening initiatives for the expansion of tests for other treatable Rare Diseases<\/li><\/ul>\n\n\n\n<div class=\"wp-container-1 wp-block-buttons\">\n<div class=\"wp-block-button my-5\"><a class=\"wp-block-button__link has-white-color has-text-color has-background no-border-radius\" style=\"background-color:#7b67ab\">Contact Us<br>to discuss a personalized testing panel<\/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>View our complete screening panel with 70+ disorders<\/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>Amino Acid Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Argininosuccinic Aciduria<br>Citrullinemia, Type I<br>Citrullinemia, Type II<br>Classic Phenylketonuria<br>Homocystinuria<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Hypermethioninemia<br>Benign hyperphenylalaninemia<br>Maple Syrup Urine Disease<br>Tyrosinemia, Type I (Succinylacetone; SUAC)<br>Tyrosinemia, Type 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>Fatty Acid Oxidation Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Carnitine Uptake Defect\/Carnitine Transport Defect<br>Medium-chain Acyl-CoA dehydrogenase deficiency<br>Very long-chain Acyl-CoA dehydrogenase deficiency<br>Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency<br>Trifunctional protein deficiency<br>Short-chain acyl-CoA dehydrogenase deficiency<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Medium\/short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency<br>Medium-chain ketoacyl-CoA thiolase deficiency<br>2,4 Dienoyl-CoA reductase deficiency<br>Carnitine palmitoyltransferase Type I deficiency<br>Carnitine palmitoyltransferase Type II deficiency<br>Carnitine acylcarnitine translocase deficiency<\/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>Organic Acid Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Propionic acidemia<br>Methylmalonic acidemia (methylmalonyl-CoA mutase)<br>Methylmalonic acidemia (Cobalamin disorders)<br>Isovaleric acidemia<br>3-Methylcrotonyl-CoA carboxylase deficiency<br>3-Hydroxy-3-methylglutaric aciduria<br>Holocarboxylase synthetase deficiency<br>\u00df-Ketothiolase deficiency<br>Glutaric acidemia Type I<br>Glutaric acidemia Type II<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Methylmalonic acidemia with homocystinuria<br>Malonic acidemia<br>Isobutyryl-CoA dehydrogenase deficiency<br>2-methylbutyryl-CoA dehydrogenase deficiency<br>3-Methylglutaconic aciduria Type I<br>2-Methyl-3-hydroxybutyric aciduria<br>3-Methylglutaconic aciduria Type II, III, IV, V<br>Combined malonic and methylmalonic aciduria<br>Ornithine transcarbamylase deficiency<\/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>Lysosomal Storage Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Fabry<br>Gaucher<br>Pompe<br>Krabbe<br>Niemann-Pick A \/ B<br>Mucopolysaccharidosis I<br>Mucopolysaccharidosis II<br>Mucopolysaccharidosis IIIB<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Mucopolysaccharidosis IVA<br>Mucopolysaccharidosis IVB<br>Mucopolysaccharidosis VI<br>Mucopolysaccharidosis VII<br>\u03b1-Mannosidase<br>Neuronal Ceroid Lipofuscinosis 1<br>Neuronal Ceroid Lipofuscinosis 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>Severe Combined Immunodeficiencies<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>TREC and KREC testing for T- and B-Cell immunodeficiencies<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Adenosine deaminase (ADA) deficiency<\/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>Endocrine Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Primary congenital hypothyroidism<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Congenital adrenal hyperplasia<\/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>Neuromuscular and Peroxisomal Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>5q-Spinal Muscular Atrophy<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>X-linked Adrenoleukodystrophy<\/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>Additional Disorders<\/h4>\n\n\n\n<div class=\"wp-block-columns\">\n<div class=\"wp-block-column\">\n<p>Biotinidase deficiency<br>Classic Galactosemia (Galactosemia Type I)<br>Glucose-6-phosphate dehydrogenase deficiency<\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column\">\n<p>Cystic Fibrosis<br>Sickle Cell Disease<br>Cerebrotinous Xanthomatosis (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 my-5\"><a class=\"wp-block-button__link has-white-color has-text-color has-background no-border-radius\" href=\"mailto:info@archimedlife.com\" style=\"background-color:#7b67ab\">Contact Us<br>to discuss a personalized testing panel<\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>The&nbsp;Baby Health Check&nbsp;screening program delivers comprehensive analysis with the flexibility to personalize your screening program. What are Your Benefits of a Personalized Screening Panel? Access to Newborn Screening for more diseases in addition to those which may be provided by local screening programs Faster disease identification in difficult cases (e.g. known family history of disease)<\/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":"The&nbsp;Baby Health Check&nbsp;screening program delivers comprehensive analysis with the flexibility to personalize your screening program. What are Your Benefits of a Personalized Screening Panel? Access to Newborn Screening for more diseases in addition to those which may be provided by local screening programs Faster disease identification in difficult cases (e.g. known family history of disease)","_links":{"self":[{"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages\/6729"}],"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=6729"}],"version-history":[{"count":2,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages\/6729\/revisions"}],"predecessor-version":[{"id":7276,"href":"https:\/\/www.babyhealthcheck.com\/at\/wp-json\/wp\/v2\/pages\/6729\/revisions\/7276"}],"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=6729"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}