Why genetic screening matters
Every sperm donor at Fertilité undergoes a thorough genetic carrier screening panel that tests for hundreds of inherited conditions, including cystic fibrosis, spinal muscular atrophy, thalassaemia, and fragile X syndrome. This greatly reduces the risk of passing on serious genetic disorders to offspring.
What we screen for
- Autosomal recessive conditions (e.g., cystic fibrosis)
- X‑linked disorders (e.g., fragile X)
- Chromosomal abnormalities through karyotyping
Peace of Mind
Our genetic screening, combined with a detailed family history, ensures that only the healthiest donors are accepted. This gives recipients confidence in the safety of their chosen donor.
The Testing Process
Donors provide a blood or saliva sample. Results take approximately 2‑3 weeks. Carriers of certain conditions may still be accepted depending on the specific inheritance pattern.