{"product_id":"ebogenes-newborn-rare-disease-genetic-screening-kit","title":"EBOGENES Newborn Rare Disease Genetic Screening Kit","description":"\u003cp\u003eA saliva or cheek-swab genetic screening test for selected inherited (monogenic) rare diseases in newborns. Panel options to be provided by the laboratory.\u003c\/p\u003e\u003ch3\u003eWhat it tests\u003c\/h3\u003e\u003cp\u003eEarly-onset and clinically actionable rare genetic disorders, including inherited metabolic diseases (e.g., PKU, Pompe disease), primary immunodeficiencies (e.g., SCID), spinal muscular atrophy (SMA), cystic fibrosis (CF), and genetic hearing loss.\u003c\/p\u003e\u003ch3\u003eHow it works\u003c\/h3\u003e\u003cp\u003eOrder online → saliva collection kit is shipped to you → collect at home and send it back with the prepaid FedEx return envelope → laboratory analysis → report delivered as a PDF in your EBOGENES customer portal or by email.\u003c\/p\u003e\u003ch3\u003eWhat's in the box\u003c\/h3\u003e\u003cp\u003eSaliva \/ mouth-swab collection kit, instructions, prepaid FedEx return envelope\u003c\/p\u003e\u003ch3\u003eAt a glance\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSample:\u003c\/strong\u003e Saliva or mouth swab\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCollection:\u003c\/strong\u003e Home\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eReport time:\u003c\/strong\u003e Available 4–6 weeks after the laboratory receives your sample.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eTest type:\u003c\/strong\u003e Screening\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eWho it is for:\u003c\/strong\u003e Newborns (ordered by parents)\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch3\u003eStorage \u0026amp; handling\u003c\/h3\u003e\u003cp\u003eUnused kit: store at room temperature (15–25 °C) in a dry place, away from direct sunlight. Do not freeze. Use before the expiry date printed on the kit. After collection: keep the sealed tube at room temperature and ship it within 3 days\u003c\/p\u003e\u003ch3\u003eLaboratory \u0026amp; report\u003c\/h3\u003e\u003cp\u003eLaboratory analysis: an accredited partner laboratory. Report prepared by the EBOGENES science team and reviewed by a licensed physician.\u003c\/p\u003e\u003ch3\u003eFAQ\u003c\/h3\u003e\u003cp\u003e\u003cstrong\u003eWhat sample do I provide and can I do it at home?\u003c\/strong\u003e A small saliva sample or mouth swab, collected at home with the kit. Collection is non-invasive and takes only a few minutes.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eHow long until I get my report?\u003c\/strong\u003e Available 4–6 weeks after the laboratory receives your sample.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIs this a diagnosis?\u003c\/strong\u003e No. It is a screening test, not a diagnosis. It does not detect all rare diseases, and a negative result does not mean your baby has no risk. Some findings may be uncertain and require clinical confirmation. Please discuss results with your healthcare provider and a genetic counsellor.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eCan this test diagnose a disease?\u003c\/strong\u003e No. It is a screening test, not a diagnosis. It identifies genetic variants associated with selected rare diseases, but it cannot confirm whether your baby has a condition. A positive result must be confirmed by clinical testing. Always discuss with your healthcare provider.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eWhat happens to my baby's data?\u003c\/strong\u003e Your baby's genetic data and report are stored in Canada. Samples are destroyed within 30 days after your report is issued, unless you consent to longer storage. You can request deletion at any time by emailing info@ebovir.ca or through your customer portal; we complete requests within 30 days, except for records we must keep by law. We never use your sample or data for research.\u003c\/p\u003e\u003cp\u003e\u003cem\u003eThis is a screening test, not a diagnosis. It does not detect all rare diseases, and a negative result does not mean your baby has no risk. Some findings may be uncertain and require clinical confirmation. Results should be discussed with your healthcare provider and a genetic counsellor. Screening \/ information test – not a diagnosis. Discuss results with your healthcare provider and a genetic counsellor\u003c\/em\u003e\u003c\/p\u003e\u003cp\u003e\u003cem\u003eData stored in Canada (AWS ca-central-1).\u003c\/em\u003e\u003c\/p\u003e","brand":"TestEasy","offers":[{"title":"Default Title","offer_id":50619216298296,"sku":null,"price":3500.0,"currency_code":"CAD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0692\/2462\/8536\/files\/rs_w_1200_h_1200_25.webp?v=1751603676","url":"https:\/\/ebogenes.com\/products\/ebogenes-newborn-rare-disease-genetic-screening-kit","provider":"Ebogenes Store","version":"1.0","type":"link"}