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糖原累积病是一种少见的遗传性代谢病。我科收治一例,兹报导如下: 患儿,男,4个月。因食后呕吐3~+月入院。生后20余天始呕吐奶汁,伴间断腹泻。日十余次。均为黄色稀水样便,无粘液,脓血。持至半月前到某医院拟作钡餐检查前禁食6h后发生“昏迷”。经输注萄萄糖液后好转。住院半月出院。三天前呕吐增重转入我院。病后无抽搐,皮肤巩膜未见黄染。患儿系第三胎第三产。第一、二胎人工流产。母乳喂养,未加辅食。至今不能抬头,不会笑。父母非近亲。家族中无类似疾病史。
Glycogen storage disease is a rare inherited metabolic disease. My department admitted a case, it is reported as follows: children, male, 4 months. 3 months after eating vomiting due to hospitalization. More than 20 days after birth vomit milk, with intermittent diarrhea. More than ten times. All are yellow watery stool, no mucus, pus and blood. Half a month ago to a hospital for barium meal to be checked before the fasting 6h after the occurrence of “coma.” After the infusion of glucose solution improved. Hospital discharged half a month. Three days ago vomiting weight gain into our hospital. No convulsions after the illness, the skin sclera no yellow dye. Pediatric third-third child. First, the second abortion. Breastfeeding without food supplement. So far can not look up, will not laugh. Parents are not close relatives. No similar family history of disease.