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Quantitative MR Markers and Psychiatric Symptoms in a Patient with Fahr Disease

Patient: Female, 43 Final Diagnosis: Fahr disease Symptoms: Movement disorder • chorea and tremors • cognitive deficit • behavioral aggressiveness and restlessness • visual hallucination Medication: Haloperidolo • levomepromazine • sodium valproate Clinical Procedure: Neurology examination • neurops...

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Detalles Bibliográficos
Autores principales: Buono, Viviana Lo, Corallo, Francesco, Costa, Antonio, Bramanti, Placido, Marino, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485651/
https://www.ncbi.nlm.nih.gov/pubmed/26094250
http://dx.doi.org/10.12659/AJCR.893163
Descripción
Sumario:Patient: Female, 43 Final Diagnosis: Fahr disease Symptoms: Movement disorder • chorea and tremors • cognitive deficit • behavioral aggressiveness and restlessness • visual hallucination Medication: Haloperidolo • levomepromazine • sodium valproate Clinical Procedure: Neurology examination • neuropsychological examination • MRI Specialty: Neurology OBJECTIVE: Rare disease BACKGROUND: Fahr’s disease (FD), or primitive idiopathic calcification of the basal ganglia, is a rare neurodegenerative syndrome characterized by the presence of idiopathic bilateral and symmetrical cerebral calcifications. CASE REPORT: We describe the case of 43-year-old woman presenting with psychiatric symptoms, disorganized behavior, and migraine. Magnetic resonance imaging (MRI) examination showed basal ganglia calcifications. In addition, we analyzed the cortical brain volume and noted cortical atrophy. Extensive etiological clinico-biological assessment allowed us to exclude known causes of brain calcifications and to diagnose Fahr disease (FD). Neurological symptoms associated with psychiatric manifestations are not uncommon in FD. CONCLUSIONS: Purely psychiatric presentations are possible, as demonstrated by the present case, although there have been very few cases reported. To date, no studies related to the brain atrophy in FD have been reported.