Shulman L M, David N J, Weiner W J
Movement Disorders Center, University of Miami School of Medicine, FL 33136, USA.
Neurology. 1995 Sep;45(9):1739-43. doi: 10.1212/wnl.45.9.1739.
Niemann-Pick disease type C (NPC) is a neurometabolic genetic disorder that is distinguished from Niemann-Pick disease by its later onset, more insidious progression, variable visceromegaly, and abnormalities of intracellular cholesterol metabolism. We describe a patient who presented with an 8-year history of psychosis requiring chronic neuroleptic therapy for a presumed diagnosis of schizophrenia. He was subsequently diagnosed with NPC as the emerging features of dementia, ataxia, dysarthria, and vertical supranuclear ophthalmoplegia were recognized. The characteristic features of adult-onset NPC and the obstacles to early diagnosis are reviewed.
C型尼曼-匹克病(NPC)是一种神经代谢性遗传疾病,它与尼曼-匹克病的区别在于发病较晚、进展更为隐匿、内脏肿大情况不一以及细胞内胆固醇代谢异常。我们描述了一名患者,他有8年的精神病病史,因疑似精神分裂症而需要长期接受抗精神病药物治疗。随后,随着痴呆、共济失调、构音障碍和垂直性核上性眼肌麻痹等新出现的症状被识别出来,他被诊断为NPC。本文对成人型NPC的特征及早期诊断的障碍进行了综述。