Why chromosomal factors matter in recurrent loss
A significant portion of early pregnancy losses relate to chromosomal abnormalities in the embryo — for patients experiencing this pattern repeatedly, PGT-A screening before transfer can help identify embryos without this specific risk factor.
What PGT-A can't address
Recurrent loss has multiple possible causes beyond chromosomal factors — uterine structural issues, clotting disorders, immunological factors, and others. A thorough recurrent-loss workup, not PGT-A alone, is the appropriate starting point.
Why this deserves careful, individualized evaluation
If you've experienced recurrent loss, a comprehensive evaluation with a reproductive endocrinologist — not a single-test solution — is the responsible path forward. PGT-A may be one component of that broader evaluation, not a standalone answer.
PGT content on this site is scoped strictly to chromosomal screening (PGT-A) and known genetic disease screening (PGT-M/PGT-SR) — not sex selection or non-medical trait selection.
See colombianivf.com for a thorough evaluation with Colombia-based reproductive endocrinologists experienced in recurrent loss.
The Takeaway
If recurrent loss applies to your situation, pursue a comprehensive workup rather than assuming PGT-A alone will identify the cause — and know that support for the emotional weight of this experience matters as much as the clinical evaluation.