Whole Exome Sequencing

Testing only of the Exons (Coding Areas) of the genes, with the possibility of controlling the sick child (single) or by testing of all three Members of the Family, the Suffering Child and both Healthy Parents are subjected to this control in order to detect genetic causes of Rare Serious Neurological or other undiagnosed diseases by comparing their genomes.

Coverage> 100X, available raw data (FastQ), data review every 16 months.

ANALYTICAL FAMILY HISTORY IS REQUIRED as well as the reports of the Doctors if it is a sick person.

Response time 3-4 weeks.