Purpose of the Procedure
- Identify if partners carry mutations for recessive genetic disorders.
- Reduce the risk of having children with serious inherited conditions.
- Provide accurate data for informed reproductive decision-making.
Book Genetic Carrier Screening | Lahalak Medical Platform
Identify potential genetic risks before or during pregnancy to ensure your child's health. This comprehensive screening analyzes hundreds of genetic mutations using advanced NGS technology for maximum clinical accuracy.
Scientific name: Expanded Carrier Screening (ECS)
Advanced genetic screening for couples analyzing hundreds of recessive and X-linked conditions. Utilizing NGS technology, it assesses the risk of passing disorders to offspring, facilitating informed reproductive health planning.
Service type
Genetic Screening
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- NGS analysis for hundreds of genes
- Detailed genetic report
Medical Service Information
Who Should Get Screened?
- Couples planning for pregnancy in the near future.
- Pregnant women in early stages seeking reassurance.
- Individuals with a family history of genetic disorders.
Conditions Covered
- Cystic Fibrosis (CF).
- Sickle Cell Anemia and Thalassemia.
- Spinal Muscular Atrophy (SMA).
- Over 300 other recessive and X-linked conditions.
Conditions & Notices
- Preferably performed for both partners
- Can be done at any time during or before pregnancy
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