Evaluating the Scope of Language Impairments in a Patient with Triple X Syndrome: A Brief Report

References

• Jacobs PA, Baikie AG, Court Brown WM, MacGregor TN, Maclean N, Harnden DG. Evidence for the existence of the human” super female”. Lancet. 1959;274(7100):423–25. doi:10.1016/S0140-6736(59)90415-5.
   Google Scholar
• Tennes K, Puck M, Bryant K, Frankenburg W, Robinson A. A developmental study of girls with trisomy X. Am J Human Genet. 1975;27:71–80.
   PubMed Web of Science ®Google Scholar
• Tuke MA, Ruth KS, Wood AR, Beaumont RN, Tyrrell J, Jones SE, Collinson MN, Turner CLS, Donohoe ME, Brooke AM, et al. Mosaic Turner syndrome shows reduced penetrance in an adult population study. Genet Med. 2019;21(4):877–86. doi:10.1038/s41436-018-0271-6.
   PubMed Web of Science ®Google Scholar
• Viuff MH, Stochholm K, Uldbjerg N, Nielsen BB, Gravholt CH,, . Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for down syndrome. Human Reproduct. 2015;30(10):2419–26. doi:10.1093/humrep/dev192.
   PubMed Web of Science ®Google Scholar
• Bishop DVM, Scerif G. Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin–neurexin hypothesis. Acta Paediatr. 2011;100(6):903–07. doi:10.1111/j.1651-2227.2011.02150.x.
   PubMed Web of Science ®Google Scholar
• Otter M, Schrander-Stumpel CTRM, Curfs LMG. Triple X syndrome: a review of the literature. Eur J Hum Genet. 2010;18(3):265–71. doi:10.1038/ejhg.2009.109.
   Google Scholar
• Skuse D, Printzlau F, Wolstencroft J. Sex chromosome aneuploidies. In: Geschwind DH, Paulson HL, Klein C, editors. Handbook of clinical neurology, vol 147, neurogenetics part I. Amsterdam (Netherlands): Elsevier; 2018. p. 355–276. doi:10.1016/B978-0-444-63233-3.00024-5.
   Google Scholar
• Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L. A review of trisomy X (47, XXX). Orphanet J Rare Dis. 2010;5(1):8. doi:10.1186/1750-1172-5-8.
   PubMedGoogle Scholar
• Urbanus E, van Rijn S, Swaab H. A review of neurocognitive functioning of children with sex chromosome trisomies: identifying targets for early intervention. Clin Genet. 2020;97(1):156–67. doi:10.1111/cge.13586.
   PubMed Web of Science ®Google Scholar
• van Rijn S, Stockmann L, Borghgraef M, Bruining H, van Ravenswaaij-arts C, Govaerts L, Hansson K, Swaab H. The social behavioral phenotype in boys and girls with an extra X chromosome (Klinefelter syndrome and trisomy X): a comparison with autism spectrum disorder. J Autism Dev Disord. 2013;44(2):310–20. doi:10.1007/s10803-013-1860-5.
   Web of Science ®Google Scholar
• Netley C, Rovet J. Verbal deficits in children with 47, XXY and 47, XXX karyotypes. A Descript Exp Study Brain Lang. 1982;17:58–72. doi:10.1016/0093-934x(82)90005-0.
   PubMed Web of Science ®Google Scholar
• Pennington B, Puck M, Robinson A. Language and cognitive development in 47,XXX females followed since birth. Behav Genet. 1980;10(1):31–41. doi:10.1007/BF01067317.
   PubMed Web of Science ®Google Scholar
• Ryan TV, Crews WD Jr., Cowen L, Goering AM, Barth JT. A case of triple X syndrome manifesting with the syndrome of nonverbal learning disabilities. Child Neuropsychol. 1998;4(3):225–32. doi:10.1076/chin.4.3.225.3179.
   Web of Science ®Google Scholar
• Zampini L, Draghi L, Silibello G, Dall’Ara F, Rigamonti C, Suttora C, Zanchi P, Salerni N, Lalatta F, Vizziello P. Vocal and gestural productions of 24‐month‐old children with sex chromosome trisomies. Int J Lang Commun Disord. 2018;53(1):171–81. doi:10.1111/1460-6984.12334.
   PubMed Web of Science ®Google Scholar
• van Rijn S, Swaab H. Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX. Genet Brain Behav. 2015;14:200–08. doi:10.1111/gbb.12203.
   PubMed Web of Science ®Google Scholar
• Leggett V, Jacobs P, Nation K, Scerif G, Bishop DVM. Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review. Dev Med Child Neurol. 2010;52(2):119–29. doi:10.1111/j.1469-8749.2009.03545.x.
   PubMed Web of Science ®Google Scholar
• Bishop DVM, Brookman-Byrne A, Gratton N, Gray E, Holt G, Morgan L, Morris S, Paine E, Thornton H, Thompson PA. Language phenotypes in children with sex chromosome trisomies. Wellcome Open Res. 2019;3:143. doi:10.12688/wellcomeopenres.14904.2.
   PubMedGoogle Scholar
• Kidd E, Donnelly S, Christiansen MH. Individual differences in language acquisition and processing. Trends Cogn Sci. 2018;22(2):154–69. doi:10.1016/j.tics.2017.11.006.
   PubMed Web of Science ®Google Scholar
• Wechsler D. WAIS-III: wechsler adult intelligence scale-III, nederlandstalige bewerking. Lisse: Swets & Zeitlinger; 2001.
   Google Scholar
• Semel EM, Wiig EH, Secord W. CELF3: clinical evaluation of language fundamentals. San Antonio (TX): Psychological Corporation; 1995.
   Google Scholar
• Kort W, Schittekatte M, Compaan E. Clinical Evaluation of Language Fundamentals, Nederlandse bewerking (4e ed.; 3rd version). Amsterdam (Netherlands): Pearson Assessment and Information B.V; 2010.
   Google Scholar
• Dunn LM, Dunn LM. PPVT-III: Peabody Picture Vocabulary Test. Circle Pines (MN): American Guidance Service; 1997.
   Google Scholar
• Schlichting L.. PPVT-III-NL: Peabody Picture Vocabulary Test. Amsterdam, The Netherlands: Harcourt Assessment B.V;2005.
   Google Scholar
• Bishop DVM. The Children’s Communication Checklist—2. London (UK): Psychological Corporation; 2003.
   Google Scholar
• Geurts H.M. CCC-2-NL: Children's communication checklist-2. Amsterdam, The Netherlands: Harcourt Assessment B.V; 2007.
   Google Scholar
• Hodapp AF, Gerken KC. Correlations between scores for peabody picture vocabulary test-III and the wechsler intelligence scale for children-III. Psychol Rep. 1999;84:1139–42.
   Web of Science ®Google Scholar
• Wigby K, D'Epagnier C, Howell S, Reicks A, Wilson R, Cordeiro L, Tartaglia N. Expanding the phenotype of triple X syndrome: a comparison of prenatal versus postnatal diagnosis. American Journal of Medical Genetics PartA. 2016;170(11):2870–2881. doi: 10.1002/ajmg.a.37688.
   PubMed Web of Science ®Google Scholar
• Newbury DF, Simpson NH, Thompson PA, Bishop DVM. Stage 2 registered report: variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis. Wellcome Open Res. 2018;3(85). doi:10.12688/wellcomeopenres.14677.1.
   Google Scholar
• Fuchs D, Fuchs LS, Power MH, Dailey AM. Bias in the assessment of handicapped children. Am Educ Res J. 1985;185–98. doi:10.3102/00028312022002185.
   Web of Science ®Google Scholar
• Massa J, Gomes H, Tartter V, Wolfson V, Halperin JM. Concordance rates between parent and teacher clinical evaluation of language fundamentals observational rating scale. Int J Lang Commun Disord. 2008;43(1):99–110. doi:10.1080/13682820701261827.
   PubMed Web of Science ®Google Scholar
• Bishop DVM, Laws G, Adams C, Norbury CF. High heritability of speech and language impairments in 6-year-old twins demonstrated using parent and teacher report. Behav Genet. 2006;36(2):173–84. doi:10.1007/s10519-005-9020-0.
   PubMed Web of Science ®Google Scholar