Purpose of Screening
- Identify if parents carry silent mutations for genetic disorders.
- Assess the risk of having a child with severe inherited conditions.
- Provide couples with essential data for informed reproductive planning.
Book Expanded Genetic Screening | Lahalak Medical Platform
An advanced DNA screening for couples to detect hundreds of genetic disorders before pregnancy, minimizing the risk of inherited conditions in offspring and ensuring a healthier future for your family.
Scientific name: Expanded Genetic Carrier Screening (ECS)
A comprehensive genetic analysis screening for hundreds of mutations linked to recessive and X-linked disorders. It helps couples assess the risk of passing genetic conditions to offspring for safer family planning.
Service type
Genetic laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- DNA sequencing analysis
- Detailed genetic risk report
Medical Service Information
Who Should Get Tested?
- Couples planning to conceive in the near future.
- Individuals with a family history of genetic abnormalities.
- Consanguineous couples (related by blood) to mitigate recessive risks.
Key Disorders Covered
- Cystic Fibrosis and associated organ complications.
- Spinal Muscular Atrophy (SMA).
- Sickle Cell Anemia and Thalassemia variants.
- Over 200 other autosomal recessive and X-linked conditions.
Conditions & Notices
- Preferably performed pre-conception or in early pregnancy stages
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