PRENATAL TESTS
A reliable non-invasive test based on maternal blood designed to rule out the possibility of Down syndrome and other types of fetal trisomy from the 11th week of pregnancy.
TRISOMY price 800 BGN
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Estimated sex of the fetus
TRISOMY XY price 850 BGN
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Estimated sex of the fetus
- Turner syndrome (45 X)
- Klinefelter’s syndrome (47 XXY)
- XYY syndrome (47 XYY)
- XXX syndrome (47 XXX)
TRISOMY + (PLUS) price 1110 BGN
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Estimated sex of the fetus
- Turner syndrome (45 X)
- Klinefelter’s syndrome (47 XXY)
- XYY syndrome (47 XYY )
- XXX syndrome (47 XXX)
- DiGeorge syndrome (22q11)
- Prader-Willi and Angelman syndrome (15q11)
- Cat Crying Syndrome (5p15)
- 1p36 deletion syndrome
- Wolff-Hirschhorn syndrome (4p16. 3)
TRISOMY COMPLETE price 1200 lv.
Screening of all 23 pairs of fetal chromosomes to detect:
- changes in the number of whole chromosomes (trisomy, monosomy), including sex chromosomes;
- changes in the number of parts of each of the 23 pairs of chromosomes (duplications, deletions) at the subchromosomal level; *
- high risk of more than 100 known subchromosomal aberrations associated with known severe syndromes,
- estimated sex of the fetus.
Advantages:
– the result contains an interpretation of the result in the light of the latest scientific knowledge;
– Price includes verification of a positive test result for TRISOMY Complete by the prenatal diagnostic examination GenomeScreen **
- The TRISOMY Complete test provides high accuracy in detecting aneuploidy and subchromosomal disorders on all 23 pairs of fetal chromosomes.
- It uses low-coverage whole genome sequencing technology and CE-IVD certified bioinformatics software – TRISOMY SW test (Council Directive 98/79/EC, Annex II, List B) compliant with EN ISO 13485:2016.
