{"product_id":"egcmapren","title":"Prenatal Chromosomal Microarray","description":"\u003cp\u003ePrenatal Chromosomal Microarray Analysis (CMA) is an advanced diagnostic test used to evaluate the fetal genome for copy number variations (CNVs)—that is, small gains (duplications) or losses (deletions) of chromosomal material that may not be visible under a microscope through standard karyotyping.\u003cbr\u003eCMA is recommended in several clinical situations, including:\u003cbr\u003eAbnormal fetal ultrasound findings\u003cbr\u003eRecurrent pregnancy loss\u003cbr\u003ePrevious child with genetic abnormalities\u003cbr\u003eNormal karyotype but high suspicion of genetic disorder\u003c\/p\u003e","brand":"Enigma Genomics","offers":[{"title":"Default Title","offer_id":60790440984862,"sku":"EGCMAPREN","price":2300.0,"currency_code":"SAR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-obstetrics-carrier-v1.png?v=1793571074","url":"https:\/\/shop.enigmagenomics.com\/products\/egcmapren","provider":"Enigma Genomics","version":"1.0","type":"link"}