Prenatal and gynecological molecular diagnostics
AGC laboratory provides you with a service of non-invasive prenatal diagnostics - Veriseq NIPT® test which can be used to identify from the mother's blood the three most common genetic syndromes - Down sy., Edwards sy. I Patau sy. In addition, the Veriseq NIPT® test can be used to determine the sex of the fetus.
In addition to the above, in the AGC laboratory it is possible to perform genetic analysis of thrombophilia, which is a common cause of recurrent pregnancy losses, analysis of amniotic fluid trisomies, analysis of Y chromosomes in men, molecular analysis of infertility in women and men and so on.
It is intended for all couples who are unable to conceive, women who have had a miscarriage and couples who want to find out by non-invasive method from the tenth week of pregnancy whether the fetus has one of the three listed syndromes and the sex of the baby.
Services and prices
These services are recommended for accurate diagnosis of patients. Click on each one for more information.
QF-PCR - amniotic fluid analysis 300KM
QF-PCR analysis of trisomies 13, 18, 21 and XY chromosomes. Electropherogram analysis on SeqStudio Genetic Analyzer. Amniotic fluid is taken as a sample and the results are within 3 working days. The analysis is done as an alternative to karyotyping, which is more extensive and lasts longer. The method is 99.9% reliable.
Molecular analysis of SYCP3 gene 400KM (per exon)
Sequencing and analysis of up to 9 exons of the SYCP3 gene responsible for recurrent pregnancy losses. The sample is just one bottle of blood.
Molecular analysis of FOXD1 gene 400 KM (per exon)
Forkhead box D1 is a protein that in humans is encoded by the FOXD1 gene. Diseases associated with FOXD1 include Hypertrichosis Universalis Congenita, Ambras Type and Ureteral Disease.
Molecular analysis of thrombophilia | 290KM
Sequencing of six risk factors responsible for hereditary thrombophilia: MTHFR C677T, MTHFR A1298C, PAI1, Factor XIII, Factor V and Factor II. It is especially recommended for pregnant women who have a history of pregnancy loss. Blood is taken as a sample.
Molecular analysis of Y chromosome microdeletions 280KM
Analysis of AZFa, AZFb and AZFc region of Y chromosome. These regions, or microdeletions in these regions, can be the cause of the impossibility of pregnancy. Blood is taken as a sample.
Infertility Research Panel in Women 1400KM
Real-time PCR method of mutation detection on 84 genes involved in embryo implantation, signal transduction, cell cycle, coagulation, apoptosis, etc.
Molecular analysis of infertility in men 1400KM
Real-time PCR test for simultaneous analysis of 84 genes associated with spermatogenesis, fertilization, male fetal differentiation, cell cycle, etc.
PGD | By appointment
Preimplantation genetic diagnostics
Preimplantation genetic diagnostics
The test is performed on HPV positive women and mutational changes in cervical tissue are analysed. At the molecular level, the methylation (silencing) of two tumor suppressor genes is determined. A negative result guarantees the absence of the disease for at least a year. The analysis is performed from a specially designed swab that would be delivered to you by our laboratory. There are a large number of scientific articles available on this topic that we would also be happy to send you if you are interested.
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