{"id":1080,"date":"2019-12-06T05:36:02","date_gmt":"2019-12-06T10:36:02","guid":{"rendered":"https:\/\/genolife2020.flywheelsites.com\/test-depistage-porteur\/"},"modified":"2026-08-28T13:23:12","modified_gmt":"2026-08-28T17:23:12","slug":"carrier-test-genetic-diseases","status":"publish","type":"page","link":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/","title":{"rendered":"Reproductive"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row custom_bg_type=&#8221;image&#8221; custom_bg_cover=&#8221;cover&#8221; custom_bg_repeat=&#8221;no-repeat&#8221; custom_bg_position=&#8221;Center center&#8221; nav_skin=&#8221;light&#8221; consent_include=&#8221;include&#8221; custom_bg_image=&#8221;923&#8243; el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;padding-bottom&#8220;:&#8220;0&#8220;},&#8220;tablet_landscape&#8220;:{&#8220;padding-top&#8220;:&#8220;120&#8220;},&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;170&#8220;,&#8220;padding-bottom&#8220;:&#8220;30&#8220;}}&#8221; el_class=&#8221;service-hero&#8221;][vc_column el_design=&#8221;{&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;15&#8220;,&#8220;padding-right&#8220;:&#8220;15&#8220;,&#8220;padding-bottom&#8220;:&#8220;15&#8220;,&#8220;padding-left&#8220;:&#8220;15&#8220;}}&#8221; textalign_small=&#8221;tablet_portrait&#8221; width=&#8221;1\/2&#8243; css_animation=&#8221;&#8221;][vc_text_element disable_margin=&#8221;yes&#8221; force_color=&#8221;yes&#8221; css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;custom_1671621612636651&#8220;,&#8220;color&#8220;:&#8220;rgba(255,255,255,1)&#8220;}&#8221;]<img loading=\"lazy\" decoding=\"async\" class=\"wp-image-1324 size-medium alignleft\" role=\"img\" src=\"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg\" alt=\"pictogramme d\u00e9signant un service test de porteur g\u00e9n\u00e9tique\" width=\"450\" height=\"450\" \/><\/p>\n<h1>Reproductive carrier screening<\/h1>\n<p>[\/vc_text_element][\/vc_column][vc_column el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;shift-vertical&#8220;:40},&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;15&#8220;,&#8220;padding-right&#8220;:&#8220;15&#8220;,&#8220;padding-bottom&#8220;:&#8220;15&#8220;,&#8220;padding-left&#8220;:&#8220;15&#8220;,&#8220;shift-vertical&#8220;:80}}&#8221; width=&#8221;1\/2&#8243; css_animation=&#8221;&#8221; el_class=&#8221;single-services-header-box&#8221;][vc_content_box style=&#8221;style_1&#8243; hover_anim=&#8221;hover_disable&#8221; overflow=&#8221;&#8221; el_design=&#8221;{&#8220;desktop&#8220;:{&#8220;border-top&#8220;:0,&#8220;border-right&#8220;:0,&#8220;border-bottom&#8220;:0,&#8220;border-left&#8220;:0,&#8220;padding-top&#8220;:&#8220;20&#8220;,&#8220;padding-right&#8220;:&#8220;90&#8220;,&#8220;padding-bottom&#8220;:&#8220;20&#8220;,&#8220;padding-left&#8220;:&#8220;90&#8220;}}&#8221; equal_height=&#8221;&#8221; alignment=&#8221;align_right&#8221; vertical_align=&#8221;align_middle&#8221; horizontal_align=&#8221;align_center&#8221; css_animation=&#8221;&#8221; bg_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;custom_color&#8220;,&#8220;color&#8220;:&#8220;rgba(200,226,242,1)&#8220;}}&#8221; el_class=&#8221;overlap-box&#8221;][vc_text_element typography=&#8221;{&#8220;variants&#8220;:&#8220;700&#8220;,&#8220;transform&#8220;:&#8220;uppercase&#8220;,&#8220;font_size&#8220;:&#8220;15px&#8220;}&#8221; disable_margin=&#8221;yes&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;90&#8243; mobile_landscape=&#8221;80&#8243; mobile_portrait=&#8221;80&#8243; css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;custom_3995118115677565&#8220;,&#8220;color&#8220;:&#8220;#2b90ce&#8220;}&#8221;]<\/p>\n<p style=\"text-align: center;\"><strong>Genetic counselling and testing<\/strong><\/p>\n<p>[\/vc_text_element][vc_text_element typography=&#8221;{&#8220;font_family&#8220;:&#8220;18337656&#8220;,&#8220;variants&#8220;:&#8220;700&#8220;,&#8220;subsets&#8220;:&#8220;latin&#8220;,&#8220;transform&#8220;:&#8220;uppercase&#8220;,&#8220;font_size&#8220;:&#8220;25px&#8220;}&#8221; disable_margin=&#8221;yes&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;90&#8243; mobile_landscape=&#8221;80&#8243; mobile_portrait=&#8221;80&#8243; css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;custom_3995118115677565&#8220;,&#8220;color&#8220;:&#8220;#2b90ce&#8220;}&#8221;][\/vc_text_element][\/vc_content_box][\/vc_column][\/vc_row][vc_row nav_skin=&#8221;light&#8221; consent_include=&#8221;include&#8221; el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;padding-top&#8220;:&#8220;80&#8220;,&#8220;padding-bottom&#8220;:&#8220;0&#8220;},&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;100&#8220;,&#8220;padding-bottom&#8220;:&#8220;40&#8220;}}&#8221;][vc_column css_animation=&#8221;&#8221;][vc_button_link title=&#8221;Back to services&#8221; text_typography=&#8221;{&#8220;font_family&#8220;:&#8220;32928416&#8220;,&#8220;variants&#8220;:&#8220;700&#8220;,&#8220;subsets&#8220;:&#8220;latin&#8220;,&#8220;transform&#8220;:&#8220;uppercase&#8220;,&#8220;font_size&#8220;:&#8220;15px&#8220;}&#8221; link_arrow=&#8221;arrow_left&#8221; size=&#8221;5&#8243; display=&#8221;display_block&#8221; icon_pos=&#8221;icon-left&#8221; css_animation=&#8221;&#8221; link_color=&#8221;{&#8220;id&#8220;:&#8220;custom_3995118115677565&#8220;,&#8220;color&#8220;:&#8220;#2b90ce&#8220;}&#8221; link_color_h=&#8221;{&#8220;id&#8220;:&#8220;Main accent color&#8220;,&#8220;color&#8220;:&#8220;#95c11f&#8220;}&#8221; link=&#8221;url:%2Fen%2Fservices%2F%23genetic-testing|title:Services||&#8221;][vc_empty_space height=&#8221;50px&#8221; tablet_landscape=&#8221;40px&#8221; tablet_portrait=&#8221;30px&#8221;][vc_heading heading_text=&#8221;NEW: Expanded carrier screening test package&#8221; heading_wrapper=&#8221;h2&#8243; alignment=&#8221;align_left&#8221; heading_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Main accent color&#8220;,&#8220;color&#8220;:&#8220;#94d142&#8220;}}&#8221; heading_typography=&#8221;{&#8220;font_family&#8220;:&#8220;32928416&#8220;,&#8220;subsets&#8220;:&#8220;latin&#8220;}&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;80&#8243; mobile_landscape=&#8221;70&#8243; mobile_portrait=&#8221;60&#8243; css_animation=&#8221;&#8221;][vc_empty_space][vc_video link=&#8221;https:\/\/player.vimeo.com\/video\/981584083?h=11ab56fb61&#8243;][vc_empty_space height=&#8221;10px&#8221;][vc_text_element responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;90&#8243; mobile_landscape=&#8221;85&#8243; mobile_portrait=&#8221;80&#8243; css_animation=&#8221;&#8221;]Carrier screening allows future parents, including those using an egg or sperm donor, to identify the potential risks of hundreds of genetic diseases in their future child. This genetic test can screen for more than 500 genes and can be done before or during pregnancy. Even without a family history of genetic disease, it is possible to be a carrier of a serious genetic disease and be at risk of having a child with this disease. Individuals who are carriers usually have no symptoms and this is why carrier testing for genetic diseases can be important.<\/p>\n<p>Genolife is now offering a new service, making carrier screening for genetic diseases more accessible. The process will take place in 3 stages:<\/p>\n<p><strong>1) Pre-test webinar and consent<\/strong><\/p>\n<p>After payment confirmation, you will have access to our secure online portal to watch a pre-recorded webinar by one of our genetic counsellors. This webinar will provide you with all the information you need to make an informed decision regarding testing, including the limitations of the results*. A consent form must then be signed in the portal to access the test.<\/p>\n<p><strong>2) Testing on a saliva sample<\/strong><\/p>\n<p>You will receive a saliva collection kit at your home which you will then need to return to the laboratory via a pre-paid envelope. It may take up to 21 calendar days for your sample to be analyzed.<\/p>\n<p><strong>3) Post-test genetic counselling<\/strong><\/p>\n<p>Once the results are available, you will meet with one of our certified genetic counsellors by telephone or video conference to review the results in detail and discuss the implications for you and your family members. If a reproductive risk is identified, our <a href=\"https:\/\/genolife.ca\/en\/genetic-counselling\/\">genetic counsellor<\/a> will discuss the risks, the disease and the treatment options (if available) in detail as well as reproductive options. You will receive a summary letter with a copy of your result. <span style=\"letter-spacing: -0.03px;\">If you are in the context of gamete donor selection, please note that only <\/span><strong style=\"letter-spacing: -0.03px;\"><u>one<\/u><\/strong><span style=\"letter-spacing: -0.03px;\"> donor genetic profile could be evaluated within this package.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>*If you have a personal and\/or family history of genetic disease, pre-test genetic counselling is recommended, and a negative test result will have no guarantee of being able to reduce or eliminate your reproductive risk associated with this history .<\/p>\n<p><a href=\"https:\/\/genolife.clinicmaster.com\/landing?clinicId=2578&amp;lang=en-CA\">Visit our client portal<\/a> to schedule a genetic counselling appointment.[\/vc_text_element][vc_empty_space height=&#8221;80px&#8221; tablet_landscape=&#8221;70px&#8221; tablet_portrait=&#8221;60px&#8221;][vc_heading heading_text=&#8221;Learn more about carrier screening for genetic diseases&#8221; heading_wrapper=&#8221;h5&#8243; alignment=&#8221;align_left&#8221; heading_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Main accent color&#8220;,&#8220;color&#8220;:&#8220;#94d142&#8220;}}&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;80&#8243; mobile_landscape=&#8221;70&#8243; mobile_portrait=&#8221;60&#8243; css_animation=&#8221;&#8221;][vc_empty_space height=&#8221;40px&#8221; tablet_landscape=&#8221;30px&#8221; tablet_portrait=&#8221;20px&#8221;][vc_expandable_list style=&#8221;minimal&#8221; skin=&#8221;light&#8221; title_typography=&#8221;{&#8220;font_family&#8220;:&#8220;32928416&#8220;,&#8220;variants&#8220;:&#8220;600&#8220;,&#8220;subsets&#8220;:&#8220;latin&#8220;,&#8220;font_size&#8220;:&#8220;20px&#8220;}&#8221; css_animation=&#8221;&#8221; accent_color=&#8221;{&#8220;id&#8220;:&#8220;custom_color&#8220;,&#8220;color&#8220;:&#8220;rgba(213,233,245,1)&#8220;}&#8221; el_class=&#8221;c-exp-list&#8221;][vc_expandable_list_item title=&#8221;Genetic diseases screened&#8221; tab_id=&#8221;1574973904296-2-9&#8243;][vc_text_element css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221;]<span style=\"font-weight: 400;\">Each of us carries at least one genetic disease. Even though we have no symptoms or family history of this disease, we can still have a modified copy of this gene. When both parents carry a variant (or a \u201cmutation\u201d) in the same gene, their children have a 25% risk of having the disease, regardless of gender. This is called <\/span><b>autosomal recessive inheritance.<\/b><\/p>\n<p><span style=\"font-weight: 400;\">Other diseases are transmitted by a carrier mother <\/span><b>(X-linked transmission)<\/b><span style=\"font-weight: 400;\"> and usually affect their sons.<\/span><\/p>\n<p>The expanded carrier screening test covers hundreds of genetic diseases including those that are more common in certain populations due to a founder effect (e.g. Ashkenazi Jewish origin, origin from Charlevoix\/Saguenay Lac-Saint-Jean). The diseases tested are generally severe with early onset, with or without available treatments, but some could present a certain variability and expression in adulthood. Here is an example of some conditions that are part of the panel:[\/vc_text_element][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<a href=\"https:\/\/www.cysticfibrosis.ca\/about-cf\" target=\"_blank\" rel=\"noopener noreferrer\">Cystic fibrosis<\/a>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<a href=\"https:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&amp;Expert=845\" target=\"_blank\" rel=\"noopener noreferrer\">Tay-Sachs disease<\/a>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<a href=\"https:\/\/www.liver.ca\/patients-caregivers\/liver-diseases\/tyrosinemia\/\" target=\"_blank\" rel=\"noopener noreferrer\">Tyrosinemia<\/a>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<a href=\"https:\/\/muscle.ca\/discover-md\/types-of-neuromuscular-disorders\/\" target=\"_blank\" rel=\"noopener noreferrer\">Spinal muscular atrophy<\/a>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<a href=\"http:\/\/www.fragilexcanada.ca\/index.php?home&amp;lng=en\" target=\"_blank\" rel=\"noopener noreferrer\">Fragile X syndrome<\/a>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<a href=\"https:\/\/muscle.ca\/discover-md\/types-of-neuromuscular-disorders\/\" target=\"_blank\" rel=\"noopener noreferrer\">Duchenne muscular dystrophy<\/a>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]More than 500 genetic diseases &#8211; <a href=\"https:\/\/genolife.ca\/wp-content\/uploads\/2026\/06\/Test-de-porteur-liste-de-genes-Carrier-test-gene-list-2026.pdf\" target=\"_blank\" rel=\"noopener\">see the complete list here<\/a>.[\/vc_list_item][\/vc_expandable_list_item][vc_expandable_list_item title=&#8221;Examples of people who may benefit from the carrier screening package:&#8221; tab_id=&#8221;1574637235720-1-10&#8243;][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">People without specific risks who would like to know their risks of having a child with a genetic disease, or who come from a region with a known higher carrier frequency (for example, the Saguenay-Lac-Saint-Jean, Charlevoix and Haute-C\u00f4te-Nord regions, Eastern Europe or those of Ashkenazi Jewish origin, and the Mediterranean, Africa and Southeast Asia regions), or couples with consanguinity.<\/span>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">People undergoing fertility treatment who will use an egg or sperm donor who is a carrier of a genetic disease<\/span>[\/vc_list_item][\/vc_expandable_list_item][vc_expandable_list_item title=&#8221;Genetic counselling&#8221; tab_id=&#8221;1612197586596-2-9&#8243;][vc_text_element css_animation=&#8221;&#8221;]<span style=\"font-weight: 400;\">At Genolife, <\/span><span style=\"font-weight: 400;\">our genetic experts<\/span><span style=\"font-weight: 400;\"> are here to help you understand your risks and options to be able to make the best decisions regarding your reproductive risks. Our genetic counsellor can discuss with you:<\/span>[\/vc_text_element][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">The implications of your genetic test results for you and your family members<\/span>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">Your risk to have a child with a genetic disease<\/span>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">The reproductive options available to you<\/span>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">The follow-up with your physician (if applicable)<\/span>[\/vc_list_item][\/vc_expandable_list_item][vc_expandable_list_item title=&#8221;Genetic testing for carrier screening&#8221; tab_id=&#8221;1612900387742-4-4&#8243;][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">We work with clinical laboratories that are accredited to perform medical genetic testing.<\/span>[\/vc_list_item][vc_list_item css_animation=&#8221;&#8221; bullet_color=&#8221;{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}&#8221; text_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Default text color&#8220;,&#8220;color&#8220;:&#8220;#454646&#8220;}}&#8221;]<span style=\"font-weight: 400;\">A genetic test evaluates the sequence of the gene to find variants, like reading a book to find spelling mistakes. We all have genetic variants, not all of them are problematic. Certain variants, called pathogenic variants or mutations, have a large impact on the function of the gene and are associated with that disease.<\/span>[\/vc_list_item][\/vc_expandable_list_item][\/vc_expandable_list][\/vc_column][\/vc_row][vc_row nav_skin=&#8221;light&#8221; consent_include=&#8221;include&#8221;][vc_column el_design=&#8221;{&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;25&#8220;,&#8220;padding-right&#8220;:&#8220;15&#8220;,&#8220;padding-bottom&#8220;:&#8220;25&#8220;,&#8220;padding-left&#8220;:&#8220;15&#8220;}}&#8221; css_animation=&#8221;&#8221;][vc_row_inner max_width=&#8221;800px&#8221; consent_include=&#8221;include&#8221; el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;padding-bottom&#8220;:&#8220;0&#8220;},&#8220;desktop&#8220;:{&#8220;padding-bottom&#8220;:&#8220;20px&#8220;}}&#8221;][vc_column_inner css_animation=&#8221;&#8221;][vc_heading heading_text=&#8221;Request your expanded carrier screening package here:&#8221; heading_wrapper=&#8221;h4&#8243; alignment=&#8221;align_center&#8221; heading_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;Main accent color&#8220;,&#8220;color&#8220;:&#8220;#94d142&#8220;}}&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;80&#8243; mobile_landscape=&#8221;70&#8243; mobile_portrait=&#8221;60&#8243; css_animation=&#8221;&#8221;][\/vc_column_inner][\/vc_row_inner][vc_raw_html]JTVCc2ltcGF5JTIwaWQlM0QlMjIzNjMzJTIyJTVE[\/vc_raw_html][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row custom_bg_type=&#8221;image&#8221; custom_bg_cover=&#8221;cover&#8221; custom_bg_repeat=&#8221;no-repeat&#8221; custom_bg_position=&#8221;Center center&#8221; nav_skin=&#8221;light&#8221; consent_include=&#8221;include&#8221; custom_bg_image=&#8221;923&#8243; el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;padding-bottom&#8220;:&#8220;0&#8220;},&#8220;tablet_landscape&#8220;:{&#8220;padding-top&#8220;:&#8220;120&#8220;},&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;170&#8220;,&#8220;padding-bottom&#8220;:&#8220;30&#8220;}}&#8221; el_class=&#8221;service-hero&#8221;][vc_column el_design=&#8221;{&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;15&#8220;,&#8220;padding-right&#8220;:&#8220;15&#8220;,&#8220;padding-bottom&#8220;:&#8220;15&#8220;,&#8220;padding-left&#8220;:&#8220;15&#8220;}}&#8221; textalign_small=&#8221;tablet_portrait&#8221; width=&#8221;1\/2&#8243; css_animation=&#8221;&#8221;][vc_text_element disable_margin=&#8221;yes&#8221; force_color=&#8221;yes&#8221; css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;custom_1671621612636651&#8220;,&#8220;color&#8220;:&#8220;rgba(255,255,255,1)&#8220;}&#8221;] Reproductive carrier screening [\/vc_text_element][\/vc_column][vc_column el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;shift-vertical&#8220;:40},&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;15&#8220;,&#8220;padding-right&#8220;:&#8220;15&#8220;,&#8220;padding-bottom&#8220;:&#8220;15&#8220;,&#8220;padding-left&#8220;:&#8220;15&#8220;,&#8220;shift-vertical&#8220;:80}}&#8221; width=&#8221;1\/2&#8243; css_animation=&#8221;&#8221; el_class=&#8221;single-services-header-box&#8221;][vc_content_box style=&#8221;style_1&#8243; hover_anim=&#8221;hover_disable&#8221; overflow=&#8221;&#8221; el_design=&#8221;{&#8220;desktop&#8220;:{&#8220;border-top&#8220;:0,&#8220;border-right&#8220;:0,&#8220;border-bottom&#8220;:0,&#8220;border-left&#8220;:0,&#8220;padding-top&#8220;:&#8220;20&#8220;,&#8220;padding-right&#8220;:&#8220;90&#8220;,&#8220;padding-bottom&#8220;:&#8220;20&#8220;,&#8220;padding-left&#8220;:&#8220;90&#8220;}}&#8221; equal_height=&#8221;&#8221; alignment=&#8221;align_right&#8221; vertical_align=&#8221;align_middle&#8221; horizontal_align=&#8221;align_center&#8221; css_animation=&#8221;&#8221; bg_color=&#8221;{&#8220;solid&#8220;:{&#8220;id&#8220;:&#8220;custom_color&#8220;,&#8220;color&#8220;:&#8220;rgba(200,226,242,1)&#8220;}}&#8221; el_class=&#8221;overlap-box&#8221;][vc_text_element typography=&#8221;{&#8220;variants&#8220;:&#8220;700&#8220;,&#8220;transform&#8220;:&#8220;uppercase&#8220;,&#8220;font_size&#8220;:&#8220;15px&#8220;}&#8221; disable_margin=&#8221;yes&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;90&#8243; mobile_landscape=&#8221;80&#8243; mobile_portrait=&#8221;80&#8243; css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;custom_3995118115677565&#8220;,&#8220;color&#8220;:&#8220;#2b90ce&#8220;}&#8221;] Genetic counselling and testing [\/vc_text_element][vc_text_element typography=&#8221;{&#8220;font_family&#8220;:&#8220;18337656&#8220;,&#8220;variants&#8220;:&#8220;700&#8220;,&#8220;subsets&#8220;:&#8220;latin&#8220;,&#8220;transform&#8220;:&#8220;uppercase&#8220;,&#8220;font_size&#8220;:&#8220;25px&#8220;}&#8221; disable_margin=&#8221;yes&#8221; responsiveness=&#8221;yes&#8221; tablet_portrait=&#8221;90&#8243; mobile_landscape=&#8221;80&#8243; mobile_portrait=&#8221;80&#8243; css_animation=&#8221;&#8221; color=&#8221;{&#8220;id&#8220;:&#8220;custom_3995118115677565&#8220;,&#8220;color&#8220;:&#8220;#2b90ce&#8220;}&#8221;][\/vc_text_element][\/vc_content_box][\/vc_column][\/vc_row][vc_row nav_skin=&#8221;light&#8221; consent_include=&#8221;include&#8221; el_design=&#8221;{&#8220;tablet_portrait&#8220;:{&#8220;padding-top&#8220;:&#8220;80&#8220;,&#8220;padding-bottom&#8220;:&#8220;0&#8220;},&#8220;desktop&#8220;:{&#8220;padding-top&#8220;:&#8220;100&#8220;,&#8220;padding-bottom&#8220;:&#8220;40&#8220;}}&#8221;][vc_column css_animation=&#8221;&#8221;][vc_button_link title=&#8221;Back to services&#8221; text_typography=&#8221;{&#8220;font_family&#8220;:&#8220;32928416&#8220;,&#8220;variants&#8220;:&#8220;700&#8220;,&#8220;subsets&#8220;:&#8220;latin&#8220;,&#8220;transform&#8220;:&#8220;uppercase&#8220;,&#8220;font_size&#8220;:&#8220;15px&#8220;}&#8221; link_arrow=&#8221;arrow_left&#8221; size=&#8221;5&#8243; display=&#8221;display_block&#8221; icon_pos=&#8221;icon-left&#8221; css_animation=&#8221;&#8221; link_color=&#8221;{&#8220;id&#8220;:&#8220;custom_3995118115677565&#8220;,&#8220;color&#8220;:&#8220;#2b90ce&#8220;}&#8221; link_color_h=&#8221;{&#8220;id&#8220;:&#8220;Main accent [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.3 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Carrier test for genetic diseases - Genolife - For your child&#039;s health<\/title>\n<meta name=\"description\" content=\"Even without a family history of genetic disease, it&#039;s possible to carry a serious genetic disease and pass it on to a child. Perform a carrier test today.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Carrier screening for genetic diseases | Genolife\" \/>\n<meta property=\"og:description\" content=\"Even without a family history of genetic disease, it is possible to carry a serious genetic disease and be at risk of having a child with the disease. Individuals who are carriers usually have no symptoms.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/\" \/>\n<meta property=\"og:site_name\" content=\"Genolife\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/GenolifeQC\" \/>\n<meta property=\"article:modified_time\" content=\"2026-08-28T17:23:12+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/genolife.ca\/wp-content\/uploads\/2019\/12\/genolife-facebook-2019.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" \/>\n\t<meta property=\"og:image:height\" content=\"631\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"6 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/\",\"url\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/\",\"name\":\"Carrier test for genetic diseases - Genolife - For your child's health\",\"isPartOf\":{\"@id\":\"https:\/\/genolife.ca\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#primaryimage\"},\"image\":{\"@id\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg\",\"datePublished\":\"2019-12-06T10:36:02+00:00\",\"dateModified\":\"2026-08-28T17:23:12+00:00\",\"description\":\"Even without a family history of genetic disease, it's possible to carry a serious genetic disease and pass it on to a child. Perform a carrier test today.\",\"breadcrumb\":{\"@id\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#primaryimage\",\"url\":\"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg\",\"contentUrl\":\"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/genolife.ca\/en\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Reproductive\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/genolife.ca\/#website\",\"url\":\"https:\/\/genolife.ca\/\",\"name\":\"Genolife\",\"description\":\"\",\"publisher\":{\"@id\":\"https:\/\/genolife.ca\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/genolife.ca\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/genolife.ca\/#organization\",\"name\":\"Genolife\",\"url\":\"https:\/\/genolife.ca\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/genolife.ca\/#\/schema\/logo\/image\/\",\"url\":\"https:\/\/genolife.ca\/wp-content\/uploads\/2019\/11\/genolife-logo-dark-2020.svg\",\"contentUrl\":\"https:\/\/genolife.ca\/wp-content\/uploads\/2019\/11\/genolife-logo-dark-2020.svg\",\"width\":435,\"height\":98,\"caption\":\"Genolife\"},\"image\":{\"@id\":\"https:\/\/genolife.ca\/#\/schema\/logo\/image\/\"},\"sameAs\":[\"https:\/\/www.facebook.com\/GenolifeQC\",\"https:\/\/www.instagram.com\/genolife_santegenetique\/\"]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Carrier test for genetic diseases - Genolife - For your child's health","description":"Even without a family history of genetic disease, it's possible to carry a serious genetic disease and pass it on to a child. Perform a carrier test today.","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:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/","og_locale":"en_US","og_type":"article","og_title":"Carrier screening for genetic diseases | Genolife","og_description":"Even without a family history of genetic disease, it is possible to carry a serious genetic disease and be at risk of having a child with the disease. Individuals who are carriers usually have no symptoms.","og_url":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/","og_site_name":"Genolife","article_publisher":"https:\/\/www.facebook.com\/GenolifeQC","article_modified_time":"2026-08-28T17:23:12+00:00","og_image":[{"width":1200,"height":631,"url":"https:\/\/genolife.ca\/wp-content\/uploads\/2019\/12\/genolife-facebook-2019.png","type":"image\/png"}],"twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"6 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/","url":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/","name":"Carrier test for genetic diseases - Genolife - For your child's health","isPartOf":{"@id":"https:\/\/genolife.ca\/#website"},"primaryImageOfPage":{"@id":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#primaryimage"},"image":{"@id":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#primaryimage"},"thumbnailUrl":"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg","datePublished":"2019-12-06T10:36:02+00:00","dateModified":"2026-08-28T17:23:12+00:00","description":"Even without a family history of genetic disease, it's possible to carry a serious genetic disease and pass it on to a child. Perform a carrier test today.","breadcrumb":{"@id":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/"]}]},{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#primaryimage","url":"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg","contentUrl":"https:\/\/genolife.ca\/wp-content\/uploads\/\/2019\/12\/genolife-picto-prenatal-blanc.svg"},{"@type":"BreadcrumbList","@id":"https:\/\/genolife.ca\/en\/carrier-test-genetic-diseases\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/genolife.ca\/en\/"},{"@type":"ListItem","position":2,"name":"Reproductive"}]},{"@type":"WebSite","@id":"https:\/\/genolife.ca\/#website","url":"https:\/\/genolife.ca\/","name":"Genolife","description":"","publisher":{"@id":"https:\/\/genolife.ca\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/genolife.ca\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/genolife.ca\/#organization","name":"Genolife","url":"https:\/\/genolife.ca\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/genolife.ca\/#\/schema\/logo\/image\/","url":"https:\/\/genolife.ca\/wp-content\/uploads\/2019\/11\/genolife-logo-dark-2020.svg","contentUrl":"https:\/\/genolife.ca\/wp-content\/uploads\/2019\/11\/genolife-logo-dark-2020.svg","width":435,"height":98,"caption":"Genolife"},"image":{"@id":"https:\/\/genolife.ca\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/www.facebook.com\/GenolifeQC","https:\/\/www.instagram.com\/genolife_santegenetique\/"]}]}},"_links":{"self":[{"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/pages\/1080"}],"collection":[{"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/comments?post=1080"}],"version-history":[{"count":0,"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/pages\/1080\/revisions"}],"wp:attachment":[{"href":"https:\/\/genolife.ca\/en\/wp-json\/wp\/v2\/media?parent=1080"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}