Abstract
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.
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Communicated by: Ed Wraith
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Walterfang, M., Kornberg, A., Adams, S. et al. Post-ictal psychosis in adolescent Niemann-Pick disease type C. J Inherit Metab Dis 33 (Suppl 3), 63–65 (2010). https://doi.org/10.1007/s10545-009-9021-x
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DOI: https://doi.org/10.1007/s10545-009-9021-x