Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Public Health, Environmental and Occupational Health,Epidemiology
Link
https://link.springer.com/content/pdf/10.1007/s12687-023-00682-8.pdf
Reference43 articles.
1. Aliberti L, Gagliardi I, Bigoni S, Lupo S, Caracciolo S, Ferlini A, Isidori AM, Zatelli MC, Ambrosio MR (2022) Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who. J Community Genet:1–10. https://doi.org/10.1007/s12687-022-00585-0
2. Bardsley MZ, Kowal K, Levy C, Gosek A, Ayari N, Tartaglia N, Lahlou N, Winder B, Grimes S, Ross JL (2013) 47,XYY syndrome: clinical phenotype and timing of ascertainment. J Pediatr 163(4):1085–1094. https://doi.org/10.1016/j.jpeds.2013.05.037
3. Berglund A, Stochholm K, Gravholt CH (2020) The epidemiology of sex chromosome abnormalities. Am J Med Genet C: Semin Med Genet 184(2):202–215. https://doi.org/10.1002/ajmg.c.31805
4. Berglund A, Viuff MH, Skakkebæk A, Chang S, Stochholm K, Gravholt CH (2019) Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study. Orphanet J Rare Dis 14(1):16. https://doi.org/10.1186/s13023-018-0976-2
5. Biesecker BB, Erby L (2008) Adaptation to living with a genetic condition or risk: a mini-review. Clin Genet 74(5):401–407. https://doi.org/10.1111/j.1399-0004.2008.01088.x
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