Non-invasive prenatal test
The peace of mind you need for your pregnancy.
Know with high reliability the risk of the fetus suffering from chromosomal syndromes, syndromes related to microdeletions and dominant monogenic diseases through a test performed on maternal blood.
The prenatal genetic test on maternal blood allows the detection of chromosomal and genetic alterations with a reliability of over 99% for the diagnosis of Down’s Syndrome, Edwards’ Syndrome and Patau’s Syndrome through massive state-of-the-art sequencing and internationally approved diagnostic algorithms.
The test can offer additional information on alterations in the number or structure of all chromosomes, including the sex chromosomes.
Even so, it offers the possibility of detecting up to 38 microdeletion syndromes with a resolution of 5 MB and the search for pathogenic variants and probably associated with dominant monogenic diseases (not suitable for egg donations)* **.
What requirements must the patient meet in order to extract true information from this test?
– Having completed at least 10 weeks of confirmed pregnancy**.
– Single pregnancy.
– Not meeting criteria that advise a diagnosis by invasive test as a first choice.
Delivery date between 5 and 15 business days, depending on the number of markers analyzed.
*For more information, request documentation from the laboratory.
**A minimum of 12 weeks will be required to determine the 2038 pathogenic variants.
COLL GARCÉS LABORATORIES
-
Rocafort 67, baixos |
08015 Barcelona - 933 259 454
- 935 102 360
- info@collgarces.com
All rights reserved
COLL GARCÉS LABORATORIOS
-
Rocafort 67, baixos |
08015 Barcelona - 933 259 454
- 935 102 360
- info@collgarces.com
COLL GARCÉS
- Pruebas y tests
- Mutuas
- Centros de extracción
- Extracción a domicilio
- Tienda
- Contáctanos
- Resultados