Men’s Infertility Genetic Panel

This comprehensive panel analyzes key genetic factors that may contribute to male infertility, including mutations in genes involved in spermatogenesis and testicular function.
The panel is ideal for evaluating individuals with:
Azoospermia (no sperm)
Severe oligospermia (low sperm count)
Abnormal sperm morphology or motility
Unexplained infertility
By identifying genetic causes, this test can guide reproductive planning, eligibility for assisted reproductive technologies (ART), and inform the risk of transmission to offspring.
Key components may include:
CFTR gene mutations (linked to congenital absence of the vas deferens)
Other fertility-related genes (e.g., NR5A1, TEX11, DMRT1)