In Our Genes Lies Our Health Story! A Dive into the Importance of Carrier Screening in our Lives

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Welcome back to the second episode of “Genetic Mysteries Unravelled” by First Genomix, where we continue our exploration of the world of genetic health and testing.

In this enlightening episode, we unravel the fascinating science behind FirstScreen (Carrier Screening) – a crucial genetic test that holds the power to shape the future of our families and our health.

FirstScreen (Carrier Screening) allows individuals to understand their genetic makeup better and be aware of potential genetic conditions that they might pass on to their children. Our host, Dany Mohsen, in conversation with Zeina Younes, the Deputy Head of Genetic Diagnostics Department, discusses what it means to be a silent carrier of genetic conditions, why it's important for every individual, particularly couples planning to start a family, to undergo carrier screening, and how this can help identify the risks of having affected offspring.

Discover intriguing insights about the increased risk among related couples, the recurring percentage of risk in each pregnancy, and the kind of diseases that this test can potentially reveal. Zeina also explains the process of the test, the potential solutions for couples sharing a mutation in the same gene, and why First Genomix stands as the preferred choice for carrier screening.

This episode is a must-watch for anyone who wants to understand the impact of our genes on our health, or those looking to make informed decisions about starting a family. Don't miss this chance to gain a deeper understanding of carrier screening and the powerful role it plays in our lives.

#FirstScreen #CarrierScreening #Podcast #FirstGenomix #GeneticMysteries