{"title":"Family Planning","description":"\u003cp\u003ePlanning for a family begins with understanding your genetic health. Enigma’s Family Planning package provides advanced genetic testing solutions designed to identify inherited risks before and during pregnancy, helping individuals and couples make informed reproductive decisions.\u003c\/p\u003e\u003cp\u003eFrom premarital screening to preconception assessment and chromosome analysis, our tests support early risk identification, personalized reproductive planning, and informed decisions for a healthier future family.\u003c\/p\u003e","products":[{"product_id":"egcytkar","title":"Karyotyping","description":"The Karyotyping is designed to identify abnormalities in the number or structure of chromosomes in a person's cells. This test can be used to diagnose genetic disorders and to assess the genetic health of a fetus during pregnancy. It provides a comprehensive analysis of a person's genetic material.","brand":"Medical Genetics Company","offers":[{"title":"Default Title","offer_id":44974154547486,"sku":"EGCYTKAR","price":850.0,"currency_code":"SAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-cytogenetics-chromosome-v1.png?v=1793571413"},{"product_id":"egchymic","title":"Y Chromosome Microdeletion","description":"\u003cp\u003eThe Y Chromosome Microdeletion Test identifies small deletions in the azoospermia factor (AZF) regions of the Y chromosome (AZFa, AZFb, AZFc), which play a crucial role in sperm production. These deletions are a common genetic cause of male infertility, accounting for 5-15% of cases of non-obstructive azoospermia and severe oligospermia.\u003c\/p\u003e\u003cp\u003eThe test is performed using PCR-based methods to detect specific deletions within the AZF regions. Results provide valuable information about the potential for natural conception, the suitability of assisted reproductive techniques (e.g., ICSI), and the genetic implications for offspring. Genetic counseling is recommended for patients with confirmed Y chromosome microdeletions.\u003c\/p\u003e\u003cp\u003eThis test is essential for men experiencing infertility or poor sperm quality and supports personalized treatment and family planning decisions.\u003c\/p\u003e","brand":"Enigma Genomics","offers":[{"title":"Default Title","offer_id":60790440952094,"sku":"EGCHYMIC","price":990.0,"currency_code":"SAR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-targeted-chromosome-v1.png?v=1793571480"},{"product_id":"egexopre","title":"Comprehensive Premarital \/Carrier Screening","description":"\u003cp\u003eTo evaluate a wide range of genetic disorders that may affect reproductive health and to support informed family planning.\u003cbr\u003eCovers over 4000 AR Autosomal recessive genetic conditions.\u003cbr\u003eFocuses on autosomal recessive disorders to identify carrier status.\u003cbr\u003eHelps couples understand their potential genetic risks before marriage or conception.\u003cbr\u003eReporting:\u003cbr\u003eIndividual Reports: Each spouse receives a detailed report of their own genetic results.\u003cbr\u003eJoint Report: A combined report showing both partners’ results, providing a clear overview of potential risks for future children.\u003cbr\u003eBenefit:\u003cbr\u003eEmpowers couples to make informed decisions regarding family planning and the health of their future children.\u003cbr\u003eConditions or Mutations Included in the Test:\u003c\/p\u003e","brand":"Enigma Genomics","offers":[{"title":"Default Title","offer_id":60790441672990,"sku":"EGEXOPRE","price":2550.0,"currency_code":"SAR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/files\/enigma-test-icon-obstetrics-couple-v1.png?v=1793571081"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0748\/6678\/6590\/collections\/family-planning.jpg?v=1793881269","url":"https:\/\/shop.enigmagenomics.com\/en\/collections\/family-planning.oembed","provider":"Enigma Genomics","version":"1.0","type":"link"}