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Post-ictal psychosis in adolescent Niemann-Pick disease type C.
Walterfang, Mark; Kornberg, Andrew; Adams, Sophia; Fietz, Michael; Velakoulis, Dennis.
Affiliation
  • Walterfang M; Neuropsychiatry Unit, Royal Melbourne Hospital, Melbourne, VIC, Australia. mark.walterfang@mh.org.au
J Inherit Metab Dis ; 33 Suppl 3: S63-5, 2010 Dec.
Article in En | MEDLINE | ID: mdl-20069374
We describe the presentation of an adolescent with juvenile-onset Niemann-Pick disease type C (NPC) who presented with post-ictal psychosis in the context of a developing seizure disorder. After demonstrating mild gait disturbance beginning at the age of 4 years, he was diagnosed with NPC at age 12 on the basis of 95% of cultured fibroblasts staining positive for filipin and a reduced fibroblast cholesterol esterification rate. He then developed a seizure disorder at age 15, where clusters of seizures produced typical psychotic symptoms, including hallucinations and delusions. His seizure disorder responded to valproate, which resulted in a settling of his psychotic symptoms. Whilst post-ictal psychosis is rarely reported prior to the age of 16, NPC in adolescents and adults is particularly psychotogenic and may increase the risk for post-ictal psychosis in the pediatric population.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychotic Disorders / Seizures / Niemann-Pick Disease, Type C Type of study: Diagnostic_studies / Etiology_studies Limits: Adolescent / Humans / Male Language: En Journal: J Inherit Metab Dis Year: 2010 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychotic Disorders / Seizures / Niemann-Pick Disease, Type C Type of study: Diagnostic_studies / Etiology_studies Limits: Adolescent / Humans / Male Language: En Journal: J Inherit Metab Dis Year: 2010 Type: Article Affiliation country: Australia