Why is this test performed?
- To determine the risk of offspring inheriting serious genetic conditions.
- To help make informed reproductive decisions before pregnancy.
- To identify 'silent carriers' of recessive genetic disorders.
Book Genetic Carrier Screening in Saudi Arabia | Lahalak Medical Platform
A proactive screening for couples to detect the risk of passing recessive genetic disorders to children, ensuring informed pregnancy planning and a healthy future for your family.
Scientific name: Routine Genetic Carrier Screening
A precise laboratory analysis identifying genetic mutations for disorders like Cystic Fibrosis and SMA. It is recommended pre-conception to assess potential hereditary risks and ensure offspring safety.
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
Target Groups
- Couples planning for pregnancy in the near future.
- Individuals with a family history of hereditary diseases.
- Women seeking comprehensive routine reproductive health checks.
Common Conditions Covered
- Cystic Fibrosis.
- Spinal Muscular Atrophy (SMA).
- Sickle Cell Anemia and Thalassemia.
Conditions & Notices
- Screening both partners is recommended for accurate risk assessment
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