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粘多糖代谢病Ⅳ型(MPS-Ⅳ)是一组隐性遗传性骨软骨营养障碍性疾病,临床诊断较困难。本文报告一家系六例粘多糖Ⅳ型患者,并对粘多糖病分型及酶学研究进行了复习。
Mucopolysaccharidosis type Ⅳ (MPS-Ⅳ) is a group of recessive hereditary osteochondral dystrophy, clinical diagnosis is more difficult. This article reports a family of six cases of mucopolysaccharides Type IV patients, and mucopolysaccharide disease typing and enzymatic studies were reviewed.