Behavior Disturbance of Non-Psychiatric Etiology: A Clinical Case of Wilson’s Disease

Authors

  • David Teixeira Departamento de Psiquiatria e Saúde Mental, Centro Hospitalar Tondela-Viseu
  • Luís Isidoro Serviço de Neurologia, Centro Hospitalar Tondela-Viseu
  • João Machado Serviço de Medicina Interna, Centro Hospitalar Tondela-Viseu
  • Verónica Cabreira Serviço de Neurologia do Centro Hospitalário Universitário de São João
  • Sandra Borges Departamento de Neurociências e Saúde Mental, Faculdade de Medicina da Universidade do Porto

DOI:

https://doi.org/10.25752/psi.20910

Keywords:

Wilson’s Disease, Metabolic Diseases, Neuropsychiatry, Therapeutics, Mental Health Stigma

Abstract

Introduction: Wilson’s disease, or hepatolenticular degeneration, is a rare genetic disease associated with copper metabolism, with autosomal recessive transmission. Recognized for its dramatic systemic and neurological effects, this disease has very relevant psychiatric symptoms which are often 
underestimated.

Objectives: To describe a neuropsychiatric clinical case of Wilson’s disease, summarizing the current scientific knowledge about 
neuropsychiatric pathology in this disease.

Methods: Presentation of a clinical case with a non-systematic literature review about neuropsychiatric symptoms in Wilson’s Disease.

Results: The authors present the case of a 19-year-old woman with an early manifestation of neuropsychiatric symptoms of Wilson’s disease, whose diagnosis and initiation of treatment were postponed due to the lack of recognition of this entity and the psychiatric stigma associated with behavioral alterations.

Conclusion: A comprehensive and multisystemic medical approach should always be carried out before making a psychiatric diagnosis.

Published

2022-09-07

Issue

Section

Case Reports