"Exploring the Intersection of Heredity and Reproduction"
Reproductive Genetics is a branch of genetics that focuses on the genetic aspects of reproduction, pregnancy, and fertility. It involves the study of genetic factors that influence reproductive health, pregnancy outcomes, and the risk of genetic disorders in offspring.
Reproductive genetics encompasses various areas, including:
Preconception genetic testing: Identifying genetic carriers of inherited disorders to assess the risk of passing them to offspring.
Prenatal testing: Detecting genetic abnormalities in the fetus during pregnancy, such as Down syndrome or other chromosomal disorders.
Carrier screening:Identifying individuals with genetic mutations that could be passed on to their children.
Infertility Genetics:Studying genetic causes of infertility in both men and women, including conditions like Klinefelter syndrome, Turner syndrome, and Y chromosome micro deletions.
Genetic Causes of Recurrent Pregnancy Loss:Investigating genetic factors that may contribute to repeated miscarriages, such as chromosomal translocations in one of the parents.
Genetic counseling: Providing information and guidance to individuals and families about genetic risks and reproductive options.
Assisted reproductive technology (ART): Applying genetic principles to fertility treatments like IVF and preimplantation genetic diagnosis (PGD).
The goal of NUGENE is to empower individuals and families with knowledge about their genetic reproductive health, enabling informed decisions about family planning, pregnancy, and fertility.
