Amniocentesis is used for prenatal genetic diagnosis and fetal assessment. Procedure involves inserting needle into abdomen to sample amniotic fluid. Typically performed between 15th and 20th week of gestation. Gold standard after 15 weeks gestation for genetic disorders
CVS tests for chromosomal disorders in fetus using placental tissue sampling. First performed in Milan by Giuseppe Simoni in 1983. Usually performed at 10-12 weeks gestation, preferred before 15 weeks. Can detect over 200 disorders, primarily Down syndrome
Sonography uses high-frequency sound waves to create body images. Transducer sends waves and listens for echoes, computer translates them. Test is noninvasive and safe with no known complications
Department assists families in childbearing and healthy generations. Provides diagnosis and treatment under supervision of gynecologists and obstetricians. Offers general female health, menopause-osteoporosis and pregnancy monitoring. Organizes birth preparation courses for parents
Panorama screens for extra or missing chromosomes in baby's DNA. Only NIPT that tests for triploidy. Screening helps detect conditions like Down syndrome and microdeletions
Panorama screens for genetic conditions caused by extra or missing chromosomes. Only NIPT that tests for triploidy. Uses unique technology to distinguish between mother and baby's DNA