Comprehensive Couple Carrier Screening: Preconception Screening for a Healthier Future
Carrier screening helps couples assess their risk of passing on common genetic disorders to their future children. On average, each person carries 1-2 non-working genes that can cause severe genetic conditions. Every individual has two copies of each gene—one inherited from their mother and one from their father. A carrier has one functional and one non-functional gene copy but remains healthy, often without symptoms or a family history of the disease. Many people are unaware of their carrier status.
Protect Your Next Generation
Carrier screening is ideal for:
- Women and their partners during pregnancy (prenatal carrier screening)
- Couples with recurrent pregnancy loss, a history of miscarriage, or infertility
- Individuals with a family history of a specific genetic disorder, which can allow for more precise prenatal diagnosis
- Partners and relatives of identified carriers or individuals with the condition
- Couples planning for pregnancy (preconception carrier screening)
- Consanguineous marriages, which carry a higher risk of expressing recessive genetic conditions in offspring
Includes: Comprehensive couple carrier screening on whole exome, Pre test GC and Post test counselling
Sample: Blood sample collected from Home from both husband and wife
Genetic test conducted by renowned genetic testing lab in India.
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