It allows you to accurately diagnose the presence of chromosomal abnormalities of the fetus (e.g., Down syndrome), the most frequent genetic diseases (fragile X syndrome, cystic fibrosis, genetic deafness, thalassemia trait, Duchenne muscular dystrophy, etc.). The amniocentesis procedure can also be used to establish genetic compatibility (paternity testing) upon request. It allows you to diagnose with certainty chromosomal abnormalities of the unborn child (e.g., Down syndrome or trisomy 21), the most frequent genetic diseases (fragile X syndrome, cystic fibrosis, genetic deafness, thalassemia, Duchenne muscular dystrophy, etc.) and upon request, genetic compatibility (paternity test).