Prenatal diagnosis
Prenatal genetic testing can provide valuable information about the health of the fetus and complement the findings of sonography.
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Prenatal genetic testing can provide valuable information about the health of the fetus and complement the findings of sonography.
Unilabs Genetics performs genetic testing – screening and diagnostic - on prenatal samples (fetal cells or fetal cell-free DNA) to detect the presence of aneuploidies, monogenic diseases or other genomic structural abnormalities, thus identifying high-risk pregnancies.
Prenatal Testing
- NIPT: Tomorrow Basic (21, 18, 13, gender), Tomorrow Plus (21, 18, 13, XY, gender), Tomorrow Extended (21, 18, 13, XY, microdeletions, gender)
- Prenatal WES
- QF-PCR for chromosomes 13,18 , 21, X and Y aneuploidies
- aCGH:
Array comparative genomic hybridization (aCGH) is a high resolution analytical method which allows a thorough and comprehensive study of the whole genome. It has the ability to simultaneously detect aneuploidies, deletions, duplications, and copy neutral events such as Loss of Heterozygosity (LoH) and uniparental disomy (UPD).
The solutions provided by Unilabs Genetics has the highest analytical resolution and are further validated with the clinical interpretation of results by our medical geneticists.
- Karyotyping
We perform Chromosome Analysis (Karyotype) on amniotic fluid or chorionic villus samples to detect chromosomal aneuploidies, imbalances and rearrangements in the fetal DNA.
Please use the search box at the top of the page to search for specific tests and disorders.
If you cannot find the test you are interested in, please contact us at genetics.customercare@unilabs.com
