15/07/2026
🧬 Most carriers have no symptoms. Most have no family history.
Most people who carry an inherited genetic variant are completely healthy and have no idea they are carriers.
If both partners carry a pathogenic variant in the same gene, there is a chance of having a child with a serious inherited genetic condition, such as spinal muscular atrophy (SMA), cystic fibrosis (CF) or sickle cell disease.
Genetic carrier screening can be performed before or during pregnancy, although testing before conception provides the greatest range of reproductive options.
At Innermost Healthcare, we don’t believe one test suits everyone. We offer a choice of leading carrier screening programmes, including:
🧬 Natera Horizon™ (4, 27, 274 and 613-gene panels)
🧬 Medicover Adventia™ Expanded Carrier Screening
🧬 Fulgent Beacon® Expanded Carrier Screening
🧬 BioArray Expanded Carrier Screening
✔ Consultant-led advice before and after testing
✔ Home testing available for many patients
✔ Suitable before or during pregnancy
✔ No laboratory fee for partner testing if the first partner is identified as a carrier (subject to laboratory policy)
Whether you’re planning a pregnancy or are already expecting, carrier screening can provide valuable information about the chance of your baby inheriting certain genetic conditions and help inform your reproductive choices.
Find out more:
https://innermosthealthcare.com/pre-pregnancy/carrier-screening/