Purpose of the Screening
- Determining if parents carry genetic mutations for inherited diseases.
- Assessing the risk of offspring inheriting serious recessive conditions.
- Providing essential data for informed reproductive choices.
Book Expanded Genetic Carrier Screening in Saudi Arabia | Lahalak Medical Platform
A comprehensive genetic screening that analyzes hundreds of genes to detect the risk of passing inherited disorders to children, empowering couples with essential knowledge for informed reproductive planning and family health.
Scientific name: Expanded Genetic Carrier Screening
An advanced blood test screening for genetic mutations of common recessive disorders like Cystic Fibrosis and SMA. It assesses reproductive risks before or during pregnancy to ensure the health of future generations.
Service type
Laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- DNA analysis
- Detailed genetic report
Medical Service Information
Key Conditions Covered
- Cystic Fibrosis (CF).
- Spinal Muscular Atrophy (SMA).
- Thalassemia and Sickle Cell Disease.
- Fragile X Syndrome.
Who Should Get Tested
- Couples planning for marriage or pregnancy.
- Individuals with a family history of genetic disorders.
- Consanguineous couples (related by blood).
- Anyone seeking proactive family health planning.
Conditions & Notices
- No specific prerequisites
- Providing previous family genetic reports is recommended
Medical services you might also like
