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Pharmacopsychiatry ; 39(5): 193-4, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16944412

ABSTRACT

Neuroacanthocytois is a rare hereditary disease, which causes a degeneration of the striatum. Patients develop a choreatic movement disorder and also complex psychiatric symptoms, such as psychosis or Tourette's syndrome. We report a case of obsessive-compulsive disorder due to neuroacanthocytosis. The striatum plays an important role in the pathophysiology of obsessive-compulsive disorder. In Huntington's disease we also find obsessive-compulsive disorders, due to impairment of the fronto-striatal loop. Encouraged by similar pathophysiology and promising reports of selective serotonin reuptake inhibitors in this disease, we started a treatment with citalopram to which the patient responded very well.


Subject(s)
Chorea/complications , Citalopram/therapeutic use , Obsessive-Compulsive Disorder/drug therapy , Selective Serotonin Reuptake Inhibitors/therapeutic use , Adult , Humans , Male , Obsessive-Compulsive Disorder/etiology , Severity of Illness Index , Treatment Outcome
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