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Is genetic testing right for my child?

Answer a few quick questions about your child’s symptoms to see if exome or genome testing could help.

Let’s explore what’s next.

Based on your answers, exome or genome testing could be an important next step for your child.

Leading medical organizations, like the American College of Medical Genetics and Genomics (ACMG) and the National Society of Genetic Counselors (NSGC), recommend this type of testing as a first-line option for children with the symptoms you selected.^1,2

While your child has had genetic testing before, exome or genome testing could still make a big difference in finding answers and getting better care:

Exome and genome tests are over 2x more likely to lead to a diagnosis than chromosomal microarray.³

23% of diagnoses made through exome testing wouldn’t have been found with a multi-gene panel.⁴

If you still don’t have answers, exome or genome testing could help.

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These results should be discussed with your healthcare provider.

References: 1. Manickam K, et al. Genet Med. 2021;23(11):2029-2037. doi: 10.1038/s41436-021-01242. 2. Smith L, et al. J Genet Couns. 2022 Oct 24. Doi.org/10.1002/jgc4.1646. 3. Savatt JM, Myers SM. Front Pediatr. 2021 Feb 19;9:526779. doi: 10.3389/fped.2021.52679. eCollection 2021. doi: 10.3389/fped.2021.526779. 4. Dillon OJ, et al. Eur J Hum Genet. 2018 May;26(5):644-651. doi: 10.1038/s41431-018-0099-1. Epub 2018 Feb 16.