What types of samples can be taken in a fetal DNA test?
Publicado el: 04/08/2024
The number one fear that a mother has before deciding to perform a fetal DNA test is that the analysis will cause disorders in the pregnancy of her future child. In many cases, this fear overcomes the desire to resolve a big question such as the possibilities of knowing if there is a congenital defect.
There is no doubt that performing a good fetal DNA test requires trusting the services of a laboratory that has the latest technology, expert and qualified technicians, and a total seriousness when working to obtain accurate results. LabGenetics is perhaps the best positioned option in all aspects, as confirmed by its numerous clients.
How is a fetal DNA test performed? If you are in a high-risk pregnancy or need to satisfy a curiosity that is far from trivial, the doubts that will probably hinder your interest have to do with the process that will be developed by LabGenetics or another specialized center. We will be transparent with you, explaining it below.
Two types of fetal DNA test
In our laboratory we work with two types of fetal DNA test, although each of them is decided by our professionals based on each particular case. First, it can be performed by taking samples of chorionic villus between weeks 10 and 12 of gestation, via the uterus, by chorionic biopsy. The other option is to use amniotic fluid samples between weeks 14 and 20 of gestation, using a process called amniocentesis, by transabdominal puncture.
Once your doubts, or part of them, have been resolved, we offer to continue helping you in making your decision. Contact LabGenetics and find out about the fetal DNA test and its prices, knowing that choosing us means betting on reliability and safety for your child.
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LabGenetics offers a comprehensive, personalized, and flexible genetic diagnostic service tailored to the needs of healthcare professionals, continuously introducing new genetic diagnoses of hereditary and rare diseases into its service portfolio. Our goal is to establish close collaborations to achieve accurate and suitable results for each case as quickly and cost-effectively as possible.
Additionally, we have pioneering professionals in performing DNA paternity and maternity tests, both informational and with legal validity, as well as prenatal and postmortem tests.
We also conduct kinship tests such as grandparentage, mitochondrial DNA for maternal lineage studies, Y chromosome for paternal lineage studies, and complex kinship studies using autosomal STRs, genetic footprints, biological fluid detection, and biological criminalistics, ancestry studies, and DNA tests for individuals affected by irregular adoptions or newborn abductions.