Hemophiliacs can have healthy babies with the help of prenatal diagnosis and three-generation IVF.
1. Prenatal diagnosis: Prenatal diagnosis of amniotic fluid, chorionic villi and umbilical cord blood before delivery can test the DNA of fetal cells to see if there is any hemophilia mutation, and if there is no hemophilia gene, hemophilia carriers may be able to have healthy babies.
2. Three-generation IVF technology: hemophilia is a hereditary disease, related to gene fragments. Three-generation IVF technology requires genetic screening, which can screen healthy embryos without hemophilia gene fragments from cultured embryos for embryo transfer, which may also give birth to a healthy baby.
Hemophilia carriers need to strengthen communication with their doctors during the process of preparation and pregnancy, and undergo regular relevant checkups, so that they can also intervene in a timely manner if the doctor finds any abnormalities.