What is prenatal testing for hemophilia?

Prenatal testing for hemophilia involves genetic tests conducted during pregnancy to determine if the fetus has inherited the condition. This is typically done through techniques such as chorionic villus sampling (CVS) or amniocentesis, which analyze fetal DNA for mutations in the genes responsible for hemophilia. The testing can help expecting parents make informed decisions about the pregnancy and prepare for potential medical needs. It is particularly relevant for families with a history of hemophilia, as the condition is often inherited in an X-linked manner.