Diagnosis typically involves a comprehensive evaluation that includes:
Medical history: Detailed review of the couple's medical, surgical, and reproductive histories. Genetic testing: Karyotyping to identify chromosomal abnormalities in both partners. Ultrasound: To detect uterine abnormalities or other structural issues. Blood tests: To check for hormonal imbalances, autoimmune conditions, and blood clotting disorders. Endometrial biopsy: Sometimes performed to assess the uterine lining.
