It takes up to 8 years to diagnose children with rare complex genetic diseases. By the time the diagnosis is reached, the health of these patients has typically considerably deteriorated. Therefore, the American College of Medical Genetics and Genomics recommends using whole-exome sequencing as a first-tier test for children with complex genetic diseases. MyChildCare is designed to test all Genes at once, thus representing a quick and effective way to establish the diagnosis in a timely manner.
