PGS and PGT Tests

PGS (preimplantation genetic screening) and PGT (preimplantation genetic diagnosis). Embryo selection without genetic illnesses and chromosome alterations before its implantation. It can be described with the analysis of 5 chromosomes:

Diagnóstico Genético Preimplatacional - laboratorio

PGT in 5 chromosomes (X, Y, 13, 18, 21):

– (X, Y) Gender selection

– (13) Patau Syndrome

– (18) Edwards Syndrome

– (21) Down Syndrome

PGT in 9 chromosomes (X, Y, 13,15,16,17,18,21,22):

– Furthermore: (15, 16, 17, 22): Syndromes that cause frozen pregnancy or involuntary miscarriage among other affections (Angelman syndrome, Prader-Willi Syndrome (SPW), idic (15), trisomy 16, Li-Fraumeni syndrome, etc.)

PGT in 11 chromosomes (X, Y, 13,15,16,17,18,21,22,23 y 24):

Diagnosis of the embryo genotype related to the presence or not of the allele cause of an illness or the chromosome alteration that carry the parents. It’s recommended performing the PGT 24 when a couple has a diagnosed illness which can be inherited to their descendants.

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