肝糖元累积症为先天性糖元分解酶缺乏而成造的糖元代谢紊乱性疾病。本病早期往往不易引起人们的注意,现将长期误诊为癫痫的两例患者报道如下:病历摘要例1,女,3.5岁,一岁时出现双眼凝视,全身抽搐呈间断发作,常患腹泻,时有出冷汗,智力发育差,不会走路及说话。父母非近亲婚配,其哥出生后有类似发作,矮胖,八岁时死亡。体检:体温 Hepatic glycogen accumulation syndrome is a disorder of glycogen metabolism that is congenital glycogenolytic enzyme deficiency. This disease is often not easy to attract people’s attention early, now long-term misdiagnosed as epilepsy two cases are reported as follows: Case history summary 1, female, 3.5 years old, one year old eyes staring, systemic seizures were intermittent seizures, often diarrhea, When there is a cold sweat, poor mental development, will not walk and talk. Parents of non-relatives of marriage, his brother had a similar attack after birth, Chun-fat, died at the age of eight. Physical examination: body temperature