Genomic Diagnostics' comprehensive suite of Reproductive Health tests covers a range of investigations throughout a couple's reproductive journey.
Genetic testing can play an important role for patients planning to have a family. Genomic Diagnostics offers a broad range of genetic tests which may assist clinicians to investigate, provide answers, and guide treatment in the reproductive health setting.
In pre-pregnancy, investigations may include carrier screening for common recessive disorders, or investigations to determine infertility or sub-fertility through Y chromosome deletion testing or cystic fibrosis testing in men, or investigating premature ovarian insufficiency with fragile X testing in women.
During pregnancy, non-invasive prenatal testing (NIPT) provides the most accurate screen for chromosomal changes in the fetus. Confirmation of screening results through cytogenetic testing of amniotic fluid or chorionic villus samples may also be necessary. Genomic Diagnostics provides the full range of specialised cytogenetics tests from FISH to molecular karyotyping.
Couples experiencing recurrent miscarriage may also be investigated for potential underlying genetic causes through karyotyping.
The Reproductive Health Test Journey
Starting a family is an exciting and sometimes confusing time for your patients. There are a number of genetic tests you may like to consider for them during this process.
Select your state:
Leading the way to improved health
results in the shortest turnaround time.