When to Disclose a Borderline Incidental Finding.

Susanna McGrew, Benjamin E Berkman
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引用次数: 1

Abstract

Bourke, E., P. Snow, A. Herlihy, D. Amor, and S. Metcalfe. 2014. A qualitative exploration of mothers’ and fathers’ experiences of having a child with Klinefelter syndrome and the process of reaching this diagnosis. European Journal of Human Genetics 22 (1):18–24. doi:10.1038/ejhg.2013.102. Close, S., L. Sadler, and M. Grey. 2016. In the dark: Challenges of caring for sons with Klinefelter syndrome. Journal of Pediatric Nursing 31 (1):11–20. doi:10.1016/j. pedn.2015.05.002. Giagulli, V. A., B. Campone, M. Castellana, C. Salzano, A. D. Fisher, C. de Angelis, R. Pivonello, A. Colao, D. Pasquali, M. Maggi, et al. 2019. Neuropsychiatric aspects in men with Klinefelter syndrome. Endocrine, Metabolic & Immune Disorders Drug Targets 19 (2):109–15. doi:10. 2174/1871530318666180703160250. Johnson, L.-M., D. M. Duenas, and B. S. Wilfond. 2022. To disclose or not to disclose: Secondary findings of XXY chromosomes. The American Journal of Bioethics 22 (10): 87–88. Miller, D. T., K. Lee, A. S. Gordon, L. M. Amendola, K. Adelman, S. J. Bale, W. K. Chung, M. H. Gollob, S. M. Harrison, G. E. Herman, R. E. Hershberger, T. E. Klein, K. McKelvey, C. S. Richards, C. N. Vlangos, D. R. Stewart, M. S. Watson, and C. L. Martin. 2021. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: A policy statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine 23 (8):1391–8. doi:10.1038/s41436-021-01171-4. Miner, S. A., D. Daumler, P. Chan, A. Gupta, K. Lo, and P. Zelkowitz. 2019. Masculinity, mental health, and desire for social support among male cancer and infertility patients. American Journal of Men’s Health 13 (1):1557988318820396. doi:10.1177/15579883 18820396. Turriff, A., H. P. Levy, and B. Biesecker. 2015. Factors associated with adaptation to Klinefelter syndrome: The experience of adolescents and adults. Patient Education and Counseling 98 (1):90–5. doi:10.1016/j.pec.2014.08.012. Turriff, A., E. Macnamara, H. P. Levy, and B. Biesecker. 2017. The impact of living with Klinefelter syndrome: A qualitative exploration of adolescents and adults. Journal of Genetic Counseling 26 (4):728–37. doi:10.1007/s10897016-0041-z. Visootsak, J., N. Ayari, S. Howell, J. Lazarus, and N. Tartaglia. 2013. Timing of diagnosis of 47,XXY and 48,XXYY: A survey of parent experiences. American Journal of Medical Genetics Part A 161 (2):268–72. doi: 10.1002/ajmg.a.35709.
何时披露边缘性偶然发现。
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