Uniparental foetal disomy
Test covered by the reimbursement:
YES
Test without reimbursement:
YES
Gender:
Woman
Material:
Trophectoderm, Amplified DNA from the trophectoderm
Turnover time:
4 weeks
STATIM:
2 weeks
Material:
Trophectoderm
| Number of biopsies x 0.2 ml PCR tube with trophectoderm cells in laboratory-supplied buffer
Storage after examination: for 5 years after the report is issued -25°C – -15°C
Amplified DNA (WGA) from the trophectoderm
| 1x 0.2 ml PCR tube with aliquot of WGA product
Storage after examination: for 5 years after the report is issued -25°C – -15°C
Quick test description:
Preimplantation genetic testing aimed at demonstrating that for each pair of chromosomes, one chromosome from the father and one from the mother is present in an embryo or foetus sample.
Test details:
The test is performed by SNP array analogous to PGT by karyomapping. In addition to a foetal or embryonal sample, samples from the mother and father are included in the testing. By performing haplotype analysis, it is possible to demonstrate the presence of one chromosome of maternal or paternal origin for each pair of chromosomes.