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Case Reports in Psychiatry
Volume 2018, Article ID 3915657, 4 pages
https://doi.org/10.1155/2018/3915657
Case Report

Huntington’s Disease in a Patient Misdiagnosed as Conversion Disorder

1Department of Psychiatry and Mental Health, Setúbal Hospital Center, Rua Camilo Castelo Branco, 2910-446 Setúbal, Portugal
2Department of Neurology, Setúbal Hospital Center, Rua Camilo Castelo Branco, 2910-446 Setúbal, Portugal
3University Psychiatric Clinic, Faculdade de Medicina, Universidade de Lisboa, Avenida Professor Egas Moniz, 1649-028 Lisboa, Portugal

Correspondence should be addressed to João Machado Nogueira; moc.liamg@arieugonodahcamsolracoaoj and Ana Margarida Franco; moc.liamg@ocnarfadiragrama

João Machado Nogueira and Ana Margarida Franco contributed equally to this work.

Received 6 October 2017; Revised 4 January 2018; Accepted 22 January 2018; Published 18 February 2018

Academic Editor: Toshiya Inada

Copyright © 2018 João Machado Nogueira et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. T. Pringsheim, K. Wiltshire, L. Day, J. Dykeman, T. Steeves, and N. Jette, “The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis,” Movement Disorders, vol. 27, no. 9, pp. 1083–1091, 2012. View at Publisher · View at Google Scholar · View at Scopus
  2. D. Clark, M. M. Danzl, and E. Ulanowski, “Development of a community-based exercise program for people diagnosed and at-risk for Huntingtons disease: A clinical report,” Physiotherapy Theory and Practice, vol. 32, no. 3, pp. 232–239, 2016. View at Publisher · View at Google Scholar · View at Scopus
  3. P. J. Garcia-Ruiz, J. Garcia-Caldentey, C. Feliz, J. Del Val, A. Herranz, and J. C. Martínez-Castrillo, “Late onset Huntington's disease with 29 CAG repeat expansion,” Journal of the Neurological Sciences, vol. 363, pp. 114-115, 2016. View at Publisher · View at Google Scholar · View at Scopus
  4. A.-C. Petit, F. Hozer, K. Youssov, P. Lavaud, P. Hardy, and F. Mouaffak, “Differential response to ECT of psychotic and affective symptoms in Huntington’s disease: A case report,” The Journal of Neuropsychiatry and Clinical Neurosciences, vol. 28, no. 1, pp. e3–e5, 2016. View at Publisher · View at Google Scholar · View at Scopus
  5. J. S. Paulsen, J. D. Long, H. J. Johnson et al., “Clinical and Biomarker Changes in Premanifest Huntington Disease Show Trial Feasibility: A Decade of the PREDICT-HD Study,” Frontiers in Aging Neuroscience, vol. 6, no. 78, 2014. View at Publisher · View at Google Scholar
  6. K. A. Quaid, S. W. Eberly, E. Kayson-Rubin, D. Oakes, and I. Shoulson, “Factors related to genetic testing in adults at risk for Huntington disease: the prospective Huntington at-risk observational study (PHAROS),” Clinical Genetics, vol. 91, no. 6, pp. 824–831, 2017. View at Publisher · View at Google Scholar · View at Scopus
  7. K. Wiatr, W. J. Szlachcic, M. Trzeciak, M. Figlerowicz, and M. Figiel, “Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells,” Molecular Neurobiology, 2017. View at Publisher · View at Google Scholar
  8. J. S. Paulsen, C. Nehl, K. F. Hoth et al., “Depression and stages of Huntington's disease,” The Journal of Neuropsychiatry and Clinical Neurosciences, vol. 17, no. 4, pp. 496–502, 2005. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Gargiulo, S. Lejeune, M.-L. Tanguy et al., “Long-term outcome of presymptomatic testing in Huntington disease,” European Journal of Human Genetics, vol. 17, no. 2, pp. 165–171, 2009. View at Publisher · View at Google Scholar · View at Scopus
  10. E. van Duijn, D. Craufurd, A. A. M. Hubers et al., “Neuropsychiatric symptoms in a European Huntington's disease cohort (REGISTRY),” Journal of Neurology, Neurosurgery & Psychiatry, vol. 85, no. 12, pp. 1411–1418, 2014. View at Publisher · View at Google Scholar · View at Scopus
  11. C. Xu, J. Yogaratnam, N. Tan, and K. Sim, “Psychosis, treatment emergent extrapyramidal events, and subsequent onset of huntington's disease: A case report and review of the literature,” Clinical Psychopharmacology and Neuroscience, vol. 14, no. 3, pp. 302–304, 2016. View at Publisher · View at Google Scholar · View at Scopus
  12. K. J. Wyant, A. J. Ridder, and P. Dayalu, “Huntington’s Disease—Update on Treatments,” Current Neurology and Neuroscience Reports, vol. 17, no. 4, article no. 33, 2017. View at Publisher · View at Google Scholar · View at Scopus
  13. M. F. Mendez, “Mania in neurologic disorders,” Current Psychiatry Reports, vol. 2, no. 5, pp. 440–445, 2000. View at Publisher · View at Google Scholar
  14. A. Delval and P. Krystkowiak, “Locomotion disturbances in Huntington's disease,” Revue Neurologique, vol. 166, no. 2, pp. 213–220, 2010. View at Publisher · View at Google Scholar · View at Scopus
  15. S. S. Chaganti, E. A. McCusker, and C. T. Loy, “What do we know about late onset Huntington's disease?” Journal of Huntington’s Disease, vol. 6, no. 2, pp. 95–103, 2017. View at Publisher · View at Google Scholar · View at Scopus
  16. E. M. Coppen and R. A. C. Roos, “Current Pharmacological Approaches to Reduce Chorea in Huntington’s Disease,” Drugs, vol. 77, no. 1, pp. 29–46, 2017. View at Publisher · View at Google Scholar · View at Scopus
  17. S. Gregory, R. I. Scahill, K. K. Seunarine et al., “Neuropsychiatry and White Matter Microstructure in Huntington’s Disease,” Journal of Huntington’s Disease, vol. 4, no. 3, pp. 239–249, 2015. View at Publisher · View at Google Scholar