Non-invasive Prenatal Test
Mitochondrial DNA Test
PGT-M & PGT-SR
Online Patient Portal
Previda®-DX is a preimplantation genetic test that is designed to screen embryos for inherited genetic disorders. For couples with a family history of an inherited disease, the customized test detects specific monogenic/single gene defects (PGT-M) and chromosomal structural rearrangements (PGT-SR) in embryos. By checking for these abnormalities, Previda®-DX helps your IVF team select a healthy embryo for transfer. PGT-M and PGT-SR are both formerly known as PGD or preimplantation genetic diagnosis.
If a single gene disorder runs in your family, you can learn your child’s risk of inheriting the condition before implantation through PGT-M.
Chromosomal structural rearrangements may explain recurrent miscarriages. Screen the embryo for these abnormalities prior to transfer using our PGT-SR.
Your results can help your physician select an embryo that is free of an inherited genetic defect or unbalanced rearrangement, increasing your chance of achieving a healthy pregnancy.
At Progenesis, patients are our highest priority.
We are happy to address any of your questions or concerns.