This condition can cause severe pain, organ damage, and complications throughout a person’s life. If you or your partner carry the sickle cell trait or have a family history of SCD, you may be concerned about the risk of passing on this disease to your children.
Preimplantation Genetic Testing (PGT) offers a powerful solution to avoid SCD and increase the chances of having healthy children.
PGT-A, formerly known as PGS (Preimplantation Genetic Screening), focuses on the screening of embryos for numerical chromosomal abnormalities, known as aneuploidies. These abnormalities, such as extra or missing chromosomes, are often associated with failed implantation, miscarriages, or certain genetic disorders.
Mosaicism:
PGT-A may encounter mosaic results, where embryos exhibit a mixture of normal and abnormal cells. The clinical significance and implantation potential of mosaic embryos are still under debate, and further testing or consultation with a genetic counselor may be recommended.
Mosaicism:
PGT-A may encounter mosaic results, where embryos exhibit a mixture of normal and abnormal cells. The clinical significance and implantation potential of mosaic embryos are still under debate, and further testing or consultation with a genetic counselor may be recommended.
While PGT can greatly reduce the risk of having a child with SCD, it is important to note that no medical procedure guarantees a 100% success rate. Consulting with our fertility specialists and genetic counselors will provide you with a comprehensive understanding of the benefits, risks, and limitations of PGT for SCD.
Take control of your family’s health and future by considering PGT to avoid Sickle Cell Disease.
Contact our dedicated team today to schedule a consultation and explore the possibilities of PGT in helping you build a healthy and happy family.