We offer new services such as the new Precision Genomic Diagnosis division
We have expanded our reproductive health portfolio with this new comprehensive genetic diagnostic service that covers the entire life cycle and is supported by all available technologies (single gene, CMA, etc.) and it has more than 250 different diagnostic panels:
CGT our advanced Carrier Genetic test, the most complete Genetic screening test based on Exome sequencing that cover over 2,000 genes that cause more than 2,200 diseases, providing in 20 working days the most accurate test results to future parents giving them the opportunity to make informed decisions and review the range of options available to guide pregnancy and family planning.
Newborn Screening Test (NBS) is a comprehensive genetic test that includes 104 genes analyzed using Next Generation Sequencing (NGS) technologies allowing a direct approach of genetic disorders to reach an accurate diagnosis. It is a screening test of genetic actionable diseases indicated for all newborns and performed during the first days of life.
Connecting clinics, specialists, and patients through our digital ecosystem
In Igenomix we want to contribute by making doctor’s daily lives easier. With this idea in mind, we have developed a new Clinic Portal where specialists can manage everything which is necessary to request genetic tests, obtain documentation, request kits and even receive and download their patient’s results. Ask your local delegate for additional information!
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