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Idiopathic basal ganglia calcification presenting with obsessive-compulsive symptoms: A case report.
Yoshioka, Daisuke; Yamanashi, Takehiko; Taneda, Kenta; Matsukawa, Takashi; Orimo, Kenta; Iwata, Masaaki.
Afiliação
  • Yoshioka D; Division of Neuropsychiatry, Faculty of Medicine Tottori University Yonago Japan.
  • Yamanashi T; Division of Neuropsychiatry, Faculty of Medicine Tottori University Yonago Japan.
  • Taneda K; Division of Neurology, Faculty of Medicine Tottori University Yonago Japan.
  • Matsukawa T; Department of Neurology, Graduate School of Medicine The University of Tokyo Tokyo Japan.
  • Orimo K; Department of Neurology, Graduate School of Medicine The University of Tokyo Tokyo Japan.
  • Iwata M; Division of Neuropsychiatry, Faculty of Medicine Tottori University Yonago Japan.
PCN Rep ; 3(1): e166, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38868467
ABSTRACT

Background:

Idiopathic basal ganglia calcification (IBGC), also known as Farh's disease, is a rare neurodegenerative disorder characterized by calcification of the basal ganglia and other brain regions. This disease usually occurs in middle-aged patients and presents with various neurological and psychiatric symptoms. The exact prevalence is unknown; however, population genomic data analysis suggests a prevalence of at least 4.5/10,000 to 3.3/1000, indicating that the disease is more common than previously thought and remains underdiagnosed. Case Presentation We report the case of a middle-aged Japanese man who attempted suicide twice because of obsessive-compulsive ideation caused by trivial triggers. The patient's psychiatric symptoms resolved relatively quickly after hospitalization, and imaging and genetic testing led to a diagnosis of IBGC.

Conclusion:

This case report illustrates the importance of including IBGC in the differential diagnosis of psychiatric symptoms that initially develop in middle-aged patients.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article