Carrier Screening:
Unveiling Hidden Genetic Risks
Discover the power of Carrier Screening, a pivotal genetic test that uncovers hidden mutations potentially leading to serious genetic diseases in children, even when parents are perfectly healthy.
This crucial test is for both men and women, whether planning natural conception or embarking on assisted reproduction journeys. Understanding your genetic compatibility as a couple becomes paramount in planning for a healthy future for your offspring.
When Is Carrier Screening Recommended?
Pre-conception or early pregnancy stages
For couples aiming to gauge the risk of passing genetic mutations.
Comprehensive evaluation
For individuals assessing reproductive disorders and conditions affecting blood clotting.
Optimizing IVF treatments
By assessing a woman's response to hormone stimulation based on her genetic makeup.
What Does Carrier Screening Entail?
Carrier Screening is a sophisticated test that identifies healthy individuals carrying one or more genetic mutations. When both partners carry the same genetic mutation, there is up to a 25% chance of transmitting recessive genetic diseases to their children. These conditions include cystic fibrosis, spinal muscular atrophy, and many others. With our capability to analyze up to 2,000 genes, this test is a cornerstone in personalizing IVF treatments and ensuring the best start for your future family.
The Procedure Simplified
A simple blood test is all it takes to delve into your genetic blueprint. Results, ready within three months, provide a clear picture of your genetic health and compatibility as a couple. While it's impossible to eliminate all genetic risk, our test significantly reduces the uncertainty surrounding potential genetic disorders in your future children.
Advanced Screening Techniques
For egg or sperm donation treatments, advanced carrier screening panels are utilized to ensure genetic compatibility, minimizing the risk of recessive diseases manifesting in your child. This test surpasses legal requirements by screening for over 300 genetic diseases, offering peace of mind and a safer path to parenthood.