PGT-M Preimplantation Genetic Testing for Monogenic disorders

Who should consider using PGT-M test?

• PGT-M is indicated for patients with a  diagnosis of an autosomal dominant or X-linked single gene disease and for couples where both gamete sources are carriers of the same autosomal recessive disease.
• Igenomix has performed PGT-M for hundreds of unique genetic diseases, but some of the most frequently performed conditions include cystic fibrosis, fragile X syndrome, muscular dystrophy, and Huntington’s disease.
• If the genetic cause for any condition has been identified in the patient or a patient’s family member, Igenomix will evaluate the report and family history. 
• In most cases, Igenomix can accept the case and offer PGT-M to the patient, assuming a molecular diagnosis has been made.