{"id":3879,"date":"2022-12-05T09:50:41","date_gmt":"2022-12-05T09:50:41","guid":{"rendered":"https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/carrier-screening\/"},"modified":"2026-07-15T09:30:08","modified_gmt":"2026-07-15T09:30:08","slug":"carrier-screening","status":"publish","type":"page","link":"https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/en\/assisted-reproduction-techniques\/carrier-screening\/","title":{"rendered":"Carrier screening"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"3879\" class=\"elementor elementor-3879 elementor-545\" data-elementor-post-type=\"page\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-40150c7 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"40150c7\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-0a9b248\" data-id=\"0a9b248\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-001814e elementor-widget elementor-widget-heading\" data-id=\"001814e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">Carrier screening<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f7df4f1 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"f7df4f1\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\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-ef306e3 elementor-widget elementor-widget-text-editor\" data-id=\"ef306e3\" 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>Carrier screening consists of analysing parents to minimise the transmission of hereditary diseases to their offspring. The genetics of both parents are studied to detect possible mutations in them, and if the same mutation is found in both, decisions can be made to avoid the transmission of this disease to the baby. <\/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<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-cff4b0d elementor-section-full_width elementor-section-content-middle elementor-section-height-default elementor-section-height-default\" data-id=\"cff4b0d\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-no\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-33 elementor-top-column elementor-element elementor-element-5bbfbe0\" data-id=\"5bbfbe0\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-2a0dedd elementor-widget elementor-widget-spacer\" data-id=\"2a0dedd\" 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<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-33 elementor-top-column elementor-element elementor-element-52e9d04\" data-id=\"52e9d04\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;gradient&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap\">\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-33 elementor-top-column elementor-element elementor-element-b7adf51\" data-id=\"b7adf51\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-871eb27 elementor-widget elementor-widget-text-editor\" data-id=\"871eb27\" 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>Carrier Screening: Key to the prevention of hereditary diseases<\/h2><p>Virtually everyone carries at least one mutation associated with an inherited disease. Because these mutations are recessive, carrying one does not mean that the person has the disease. However, there is a possibility that their children may inherit it <strong style=\"font-weight: 600;\">if their reproductive partner carries the same mutation in their DNA <\/strong>and, when their genetic material combines to form the baby\u2019s genome, the baby inherits the mutated copy from both parents.<\/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-3e1d4e7 elementor-widget elementor-widget-text-editor\" data-id=\"3e1d4e7\" 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>This is because humans have all genes in duplicate, inheriting one from our mother and another from our father, and although they are the same gene, the two copies are not the same.<\/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-8cf1f2a elementor-widget elementor-widget-text-editor\" data-id=\"8cf1f2a\" 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>For this reason, in recessive diseases, <strong style=\"font-weight: 600;\">when only one of the copies has this defect, the person does not develop the disease because there is the other healthy copy.<\/strong> But if both copies are \u201cdefective\u201d, the disease manifests with its symptoms and consequences.<\/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<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-68ce6d9 elementor-section-boxed elementor-section-height-default elementor-section-height-default\" data-id=\"68ce6d9\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-default\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-114eaeb\" data-id=\"114eaeb\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-1547a19 elementor-widget elementor-widget-text-editor\" data-id=\"1547a19\" 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>What does it detect?<\/h2>\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-087ec4e elementor-widget elementor-widget-text-editor\" data-id=\"087ec4e\" 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>This test detects the presence of mutations in parents, or in donors if using donor gametes, to determine whether there is a risk of the baby having such a disease.<\/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<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-6269d56 elementor-section-full_width elementor-section-content-middle elementor-section-height-default elementor-section-height-default\" data-id=\"6269d56\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-no\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-33 elementor-top-column elementor-element elementor-element-dfca01f\" data-id=\"dfca01f\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-8863be8 elementor-widget elementor-widget-text-editor\" data-id=\"8863be8\" 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>What advantages does this test offer?<\/h2><p>The number of diseases analysed in this test ranges from 75 to more than 2200, depending on the patients. <strong style=\"font-weight: 600;\">Either the blood or saliva can be analysed, and the test is very quick and easy. Results are provided in less than a month, even in the case of genetic analysis.<\/strong><\/p><p>The great advantage of this option is that it can <strong style=\"font-weight: 600;\">minimise the risk that the baby might have a serious and dangerous disease that would condition their life or even lead to death.<\/strong><\/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<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-33 elementor-top-column elementor-element elementor-element-a38a6b6\" data-id=\"a38a6b6\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;gradient&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap\">\n\t\t\t\t\t<div class=\"elementor-background-overlay\"><\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<div class=\"elementor-column elementor-col-33 elementor-top-column elementor-element elementor-element-ccf2647\" data-id=\"ccf2647\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t<div class=\"elementor-background-overlay\"><\/div>\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-fa63782 elementor-widget elementor-widget-image\" data-id=\"fa63782\" 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=\"1996\" height=\"1902\" src=\"https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/wp-content\/uploads\/2022\/12\/Mesa-de-trabajo-1.png\" class=\"attachment-full size-full wp-image-3579\" alt=\"\" srcset=\"https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/wp-content\/uploads\/2022\/12\/Mesa-de-trabajo-1.png 1996w, https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/wp-content\/uploads\/2022\/12\/Mesa-de-trabajo-1-300x286.png 300w, https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/wp-content\/uploads\/2022\/12\/Mesa-de-trabajo-1-1024x976.png 1024w, https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/wp-content\/uploads\/2022\/12\/Mesa-de-trabajo-1-768x732.png 768w, https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/wp-content\/uploads\/2022\/12\/Mesa-de-trabajo-1-1536x1464.png 1536w\" sizes=\"(max-width: 1996px) 100vw, 1996px\" \/>\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<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Carrier screening Carrier screening consists of analysing parents to minimise the transmission of hereditary diseases to their offspring. The genetics of both parents are studied to detect possible mutations in them, and if the same mutation is found in both, decisions can be made to avoid the transmission of this disease to the baby. Carrier [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":3519,"parent":4074,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-3879","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Carrier screening - Viamed Fertility Institute<\/title>\n<meta name=\"description\" content=\"Carrier screening consists of analysing parents to minimise the transmission of hereditary diseases to their offspring.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.institutofertilidadviamed.com\/hospital-santa-angela-de-la-cruz\/en\/assisted-reproduction-techniques\/carrier-screening\/\" \/>\n<meta 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