Importance of the Test
- Identifying risks of passing rare and recessive genetic diseases.
- Providing accurate information for informed reproductive planning.
- Detecting carriers even in the absence of a family history.
Book Expanded Carrier Screening in Saudi Arabia | Lahalak Medical Platform
A comprehensive genetic screening analyzing hundreds of gene mutations before or during pregnancy to assess the risk of inherited conditions, providing peace of mind for a healthy family future.
Scientific name: Expanded Carrier Screening (ECS)
An advanced blood test screening for hundreds of autosomal recessive and X-linked genetic disorders. It helps couples understand the risk of passing inherited conditions to their children, enabling informed family planning.
Service type
Genetic laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- Analysis of hundreds of genetic mutations
- Detailed genetic report
Medical Service Information
Target Groups
- Couples planning for pregnancy soon.
- Pregnant women in their first trimester.
- Couples with a family history of genetic disorders.
What Does the Screening Cover?
- Cystic Fibrosis.
- Sickle Cell Anemia and Thalassemia.
- Spinal Muscular Atrophy (SMA).
- Hundreds of other genetic conditions.
Conditions & Notices
- Preferably performed before pregnancy or in the early stages
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