Genetic Center Services:
As part of our commitment to comprehensive care, Meya IVF Center offers a range of genetic services to help patients understand their genetic risks and make informed decisions about family planning. Our genetic center is staffed by board-certified genetic counselors and specialists who provide personalized counseling, testing, and support to individuals and families. Some of the genetic center services available at our center include:
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Genetic Counseling:
- Individualized counseling sessions to review personal and family medical histories, assess genetic risks, and discuss available testing options.
- Education and support for patients considering genetic testing for themselves or their children, including preconception screening, carrier testing, and prenatal testing.
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Carrier Screening:
- Screening tests to identify carriers of genetic mutations associated with inherited disorders such as cystic fibrosis, sickle cell disease, and spinal muscular atrophy.
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Prenatal Diagnosis:
- Prenatal testing options, including chorionic villus sampling (CVS) and amniocentesis, to diagnose genetic conditions or chromosomal abnormalities in the fetus during pregnancy.
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Preimplantation Genetic Testing (PGT):
- PGT for monogenic/single-gene disorders to screen embryos created through IVF for specific genetic mutations before implantation, reducing the risk of passing on inherited conditions to offspring.
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Genomic Medicine:
- Evaluation and interpretation of genetic test results, including whole exome sequencing (WES) and whole genome sequencing (WGS), to diagnose rare genetic disorders and guide treatment decisions.
Our genetic center services are designed to empower patients with knowledge and support as they navigate the complexities of genetic testing and family planning, ensuring that they have the information and resources they need to make informed decisions about their reproductive health.