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Developmental Neurorehabilitation Volume 15, 2012 - Issue 3
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Research Article

The psychiatric phenotype in triple X syndrome: New hypotheses illustrated in two cases

Maarten OtterDepartment of Child & Adolescent Psychiatry, ;Department of General Psychiatry, Eleos, Ede, The Netherlands;Trajectum, Community Mental Health Team in ID, Zutphen, The NetherlandsCorrespondence[email protected]
,
Constance T. R. M. Schrander-StumpelDepartment of clinical genetics, Maastricht University Medical Center UMC, Maastricht, The Netherlands;GROW School for Oncology and Developmental Biology, Maastricht University Medical Center UMC, Maastricht, The Netherlands
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Robert DiddenTrajectum, Community Mental Health Team in ID, Zutphen, The Netherlands;Behavioural Science Institute, Radboud University Nijmegen, Nijmegen, The Netherlands
&
Leopold M. G. CurfsGROW School for Oncology and Developmental Biology, Maastricht University Medical Center UMC, Maastricht, The Netherlands;Department of Clinical Genetics, Maastricht University Medical Center UMC, Maastricht, The Netherlands
Pages 233-238 | Received 29 Dec 2011, Accepted 05 Jan 2012, Published online: 14 May 2012

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Kate Attfield. (2023) ‘You don’t know how big this heart is’: parental accounts of Triple X super-daughters’ life course and emerging community citizenship. Community, Work & Family 0:0, pages 1-18.
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Articles from other publishers (11)

Maarten Otter, Bea C. M. Campforts, Constance T. R. M. Stumpel, Thérèse A. M. J. van Amelsvoort & Marjan Drukker. (2022) Triple X syndrome: Psychiatric disorders and impaired social functioning as a risk factor. European Psychiatry 66:1.
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Maarten Otter, Peter M. L. Crins, Bea C. M. Campforts, Constance T. R. M. Stumpel, Thérèse A. M. J. van Amelsvoort & Claudia Vingerhoets. (2021) Social functioning and emotion recognition in adults with triple X syndrome. BJPsych Open 7:2.
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Shanlee M. Davis, Katelyn Soares, Susan Howell, Melanie Cree-Green, Eliza Buyers, Joshua Johnson & Nicole R. Tartaglia. (2020) Diminished Ovarian Reserve in Girls and Adolescents with Trisomy X Syndrome. Reproductive Sciences 27:11, pages 1985-1991.
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Nicole Tartaglia, Susan Howell, Shanlee Davis, Karen Kowal, Tanea Tanda, Mariah Brown, Cristina Boada, Amanda Alston, Leah Crawford, Talia Thompson, Sophie Rijn, Rebecca Wilson, Jennifer Janusz & Judith Ross. (2020) Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention . American Journal of Medical Genetics Part C: Seminars in Medical Genetics 184:2, pages 428-443.
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Morten Muhlig Nielsen, Christian Trolle, Søren Vang, Henrik Hornshøj, Anne Skakkebæk, Jakob Hedegaard, Iver Nordentoft, Jakob Skou Pedersen & Claus Højbjerg Gravholt. (2020) Epigenetic and transcriptomic consequences of excess X‐chromosome material in 47, XXX syndrome—A comparison with Turner syndrome and 46, XX females . American Journal of Medical Genetics Part C: Seminars in Medical Genetics 184:2, pages 279-293.
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Antoinette am Zehnhoff-Dinnesen, Doris-Maria Denk-Linnert, Mona Hegazi, Annerose Keilmann, Christiane Kiese-Himmel, Katrin Neumann, Sabrina Regele, Rainer Schönweiler & Eva Seemanova. 2020. Phoniatrics I. Phoniatrics I 539 605 .
Tamar Green, Shira Flash & Allan L. Reiss. (2018) Sex differences in psychiatric disorders: what we can learn from sex chromosome aneuploidies. Neuropsychopharmacology 44:1, pages 9-21.
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Maarten Otter, Constance Stumpel & Therese van Amelsvoort. (2018) Client-centred clinical genetic diagnostics. Advances in Mental Health and Intellectual Disabilities 12:1, pages 1-10.
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Zi-Yan Jiang, Xiao-Hui Wu & Chao-Chun Zou. (2015) Double trisomy 48,XXX,+18 with multiple dysmorphic features. World Journal of Pediatrics 11:1, pages 83-88.
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. 2014. Benign & Pathological Chromosomal Imbalances. Benign & Pathological Chromosomal Imbalances 151 187 .
Kirstine Stochholm, Svend Juul & Claus H. Gravholt. (2013) Poor socio-economic status in 47,XXX – An unexpected effect of an extra X chromosome. European Journal of Medical Genetics 56:6, pages 286-291.
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