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粘多糖病(Mucopolysaccharidosis)亦称Hurler氏病、Hunter氏病及承(?)病(Gargoylism),1917年Hunter首先描述,我国于1955年首次报告2例,迄今国内已有170余例报道。我院儿科近年收治1例,现报告如下。一、病例报告黎××,男,7岁,住院号186,007,因腹部进行性增大伴智力低下5年,行为异常1年余,于1982年12月1日第2次入院。患儿出生后1年内生长发育基本正常,2岁时因腹胀,腹泻在当地医院就诊,发现肝大肋下4cm,肝功能检查SGPT 325u;肝脏超声波探查提示炎症波型。曾服驱虫药排出蛔虫30余条。因腹胀进行性加重,肝、脾肿大,于1978年8月第1
Mucopolysaccharidosis, also known as Hurler’s disease, Hunter’s disease and Gargoylism, was first described by Hunter in 1917. China first reported 2 cases in 1955 and so far more than 170 cases have been reported in China. Pediatric hospital in recent years, 1 case admitted, are as follows. First, the case report Lai × ×, male, 7 years old, hospital number 186,007, due to the progressive increase in the abdomen with mental retardation for 5 years, abnormal behavior more than 1 year, on December 1, 1982 2nd admission. Growth and development of children within 1 year after birth was basically normal, 2 years old due to abdominal distension and diarrhea in the local hospital, found that the large rib ribs 4cm, liver function test SGPT 325u; liver ultrasound probe indicates the wave pattern of inflammation. Served repellent excreted more than 30 roundworms. Due to progressive abdominal distension, liver, splenomegaly, in 1978 August first