Female Infertility Panel

The Female Infertility Panel is a comprehensive Next-Generation Sequencing (NGS) assay that analyzes genes associated with inherited causes of female infertility and reproductive dysfunction. The panel evaluates clinically relevant genetic variants linked to disorders such as primary ovarian insufficiency (POI), diminished ovarian reserve, oocyte maturation defects, ovarian dysgenesis, endocrine-related infertility, recurrent implantation failure, and other inherited reproductive conditions.

By identifying pathogenic variants, the panel supports the diagnosis of women with unexplained infertility, recurrent assisted reproductive technology (ART) failure, recurrent pregnancy loss with suspected genetic etiology, and a family history of reproductive disorders. Results assist clinicians in personalized fertility management, treatment planning, reproductive counseling, and informed family planning decisions.

The panel may include genes involved in:

Ovarian development and function
Folliculogenesis and oocyte maturation
Hormonal signaling pathways
Gonadal differentiation
Meiosis and DNA repair