Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2018 Apr;141(4):e20172238.
doi: 10.1542/peds.2017-2238. Epub 2018 Mar 13.

Please Test My Child for a Cancer Gene, but Don't Tell Her

Affiliations
Case Reports

Please Test My Child for a Cancer Gene, but Don't Tell Her

Johan Bester et al. Pediatrics. 2018 Apr.

Abstract

A 38-year-old woman is diagnosed with Li-Fraumeni syndrome, an autosomal dominant genetic condition that predisposes to a variety of cancers. The woman has an 11-year-old daughter. The geneticist recommends that the child be tested for the Li-Fraumeni genetic variant. The mother is concerned about the impact of testing and diagnosis on Karen's psychological well-being. She describes Karen as "highly strung" and as "a worrier." The child has been diagnosed with an anxiety disorder and is managed by a psychologist for counseling. The child is otherwise well. The mother requests that testing be done without disclosing it to the child by adding the test on to routine blood work done for another reason and requests that the results only be revealed if they are positive. Experts in genetics, law, and bioethics discuss whether it is permissible to test the child without her knowledge or assent.

PubMed Disclaimer

Conflict of interest statement

POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.

Similar articles

Cited by

References

    1. Baig SS, Strong M, Rosser E, et al. 22 Years of predictive testing for Huntington’s disease: the experience of the UK Huntington’s Prediction Consortium. Eur J Hum Genet. 2016;24:1396–402. - PMC - PubMed
    1. The World Federation of Neurology Research Group on Huntington’s Disease. Presymptomatic testing for Huntington’s disease: a world-wide survey. J Med Genet. 1993;30:1020–2. - PMC - PubMed
    1. Levin T, Mæhle L. Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma (CDKN2A) in Norway. Fam Cancer. 2017;16(2):257–265. - PMC - PubMed
    1. Fischer C, Engel C, Sutter C, et al. BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families. Clin Genet. 2012;82(5):478–83. - PubMed
    1. Clayton EW, McCullough LB, Biesecker LG, et al. Addressing the ethical challenges in genetic testing and sequencing of children. Am J Bioeth. 2014;14(3):3–9. - PMC - PubMed

Publication types