QalyGEN Exome

The QalyGEN Exome study analyzes up to 22,000 genes, with the aim of
offer better clinical diagnoses and more personalized treatments. This study
offers 1- The analysis of the 73 genes recommended by the ACMG whose mutations give rise
to diseases that can be prevented or treated. 2- Carrier screening for families
who consider pregnancy to detect the risk of hereditary diseases in children.
3- Detection of conditions in patients who present symptoms of diseases
genetic diseases that have not been diagnosed 3- Detection of congenital diseases
appearance in early childhood.