粘多糖病是一组遗传性代谢障碍病。由于粘多糖降解代谢过程中溶解体水解酶缺陷,致使粘多糖过多堆积于器官组织中,造成体格及智力发育障碍,临床上也表现出各种各样的症状,因该病比较少见,往往被误诊,现结合我院确诊的4例作一简要讨论分析。 Mucopolysaccharidosis is a group of hereditary metabolic disorders. Due to the degradation of lysozyme hydrolyzate during mucopolysaccharide degradation, resulting in excessive accumulation of mucopolysaccharide in the organ tissue, resulting in physical and mental retardation, clinical also showed a variety of symptoms, because the disease is relatively rare, often Was misdiagnosed, are now combined with the diagnosis of 4 cases in our hospital for a brief discussion and analysis.