{"product_id":"egkarppoc","title":"Prenatal Karyotyping POC","description":"\u003cp\u003ePrenatal karyotyping is a diagnostic genetic test performed on fetal cells obtained through procedures like amniocentesis or chorionic villus sampling (CVS). The goal is to analyze the fetus’s chromosomes to detect numerical abnormalities (such as extra or missing chromosomes) and large structural abnormalities, including:\u003cbr\u003eAneuploidies (e.g., trisomy 21, 18, 13)\u003cbr\u003eSex chromosome abnormalities (e.g., Turner syndrome [45,X], Klinefelter syndrome [47,XXY])\u003cbr\u003eLarge deletions or duplications\u003cbr\u003eBalanced or unbalanced translocations\u003cbr\u003eThe test involves culturing fetal cells, then staining and analyzing the chromosomes under a microscope to produce a karyogram, which is a visual representation of the chromosomes.\u003c\/p\u003e","brand":"Enigma Genomics","offers":[{"title":"Default Title","offer_id":60790444196126,"sku":"EGKARPPOC","price":2100.0,"currency_code":"SAR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-cytogenetics-carrier-v1.png?v=1793571509","url":"https:\/\/shop.enigmagenomics.com\/en\/products\/egkarppoc","provider":"Enigma Genomics","version":"1.0","type":"link"}