婴儿型高雪氏病(Gaucher’s disease)是一种较少见糖脂代谢性疾病。在我院是首例。现将我科最近收治,经临床及骨髓高雪氏细胞检查,证明为婴儿型高雪氏病,病例报告如下: 一、临床资料黄××,男,7个月,住院号16695。因反复消化不良半年,腹胀三个月,腹部触及肿块半个月于1984年7月9日住院诊治。患儿系第一胎,足月,因胎位不正行剖 Baby-type Gaucher’s disease is a less common type of glucose-lipid metabolic disorder. In our hospital is the first case. Now our department recently admitted, the clinical and bone marrow Gauch’s cell examination, proved to be infantile Gaucher disease, the case report is as follows: First, the clinical data Huang × ×, male, 7 months, hospital number 16695. Due to repeated indigestion for six months, abdominal distension for three months, half a month touching the abdomen in July 9, 1984 hospitalized. Children with the first child, full-term, due to abnormal fetal position