Genetic Tests

PGT-M at Gene Negar Ayandegan

PGT-M identifies embryos affected by a known familial monogenic disease before transfer.

← Genetic Tests

What is this test?

Disease-specific assay with custom probes tailored to the family.

When is this test recommended?

Parents who are carriers or affected with recessive/dominant diseases at high transmission risk.

Sample type

Trophectoderm biopsy and parental blood.

Results

Identification of unaffected embryos for transfer.

Limitations

Requires specialized setup and longer turnaround.

Turnaround time

To Be Added

Required documents

To Be Added

Related diseases

Thalassemia, SMA, DMD, CF, Huntington and other monogenic disorders.

Frequently Asked Questions

Contact Gene Negar Ayandegan

Contact Gene Negar Ayandegan for sample submission, laboratory collaboration, or more information.

Contact us+98 21 8821 7219

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Gene Negar Ayandegan · PGT-M at Gene Negar Ayandegan