2022年8月17日 · MPS 1 is a condition where your body doesn't have enough enzymes to break down sugar molecules (glycosaminoglycans, formerly called mucopolysaccharides). The …

2002年10月31日 · Mucopolysaccharidosis type I (MPS I) is a progressive multisystem disorder with features ranging over a continuum of severity. While affected individuals have traditionally …

Mucopolysaccharidosis type 1 (MPS 1) is a rare lysosomal storage disorder characterized by an abnormal build-up of various toxic materials, called glycosaminoglycans (GAGs) in the body's …

黏多糖贮积症Ⅰ型 (mucopolysaccharidosis type Ⅰ，MPS Ⅰ)是一种罕见的常染色体隐性遗传代谢性疾病，临床表现复杂，常累及多个器官，疾病负担重，普遍存在确诊率低、诊断延迟等情况 …

MPS I (mucopolysaccharidosis type 1 or Hurler syndrome) is an inherited condition that involves the fourth chromosome. Learn the symptoms, causes, treatment, and life expectancy of this …

Mucopolysaccharidosis type I (MPS I) is a condition that affects many parts of the body. This disorder was once divided into three separate syndromes: Hurler syndrome (MPS I-H), Hurler …

Mucopolysaccharidosis type I is a spectrum of diseases in the mucopolysaccharidosis family. It results in the buildup of glycosaminoglycans (or GAGs, or mucopolysaccharides) due to a …

黏多糖贮积症 ( mucopolysaccharidoses，MPS)，是一组罕见的 溶酶体病。 由于溶酶体内酶的缺陷或缺乏，机体分解黏多糖（长链糖分子）障碍，导致这些糖分子在细胞内、血液和结缔组织 …

2023年4月24日 · Mucopolysaccharidosis type I (MPS I) is a rare disease in which the body is missing or does not have enough of an enzyme needed to break down long chains of sugar …

黏多糖贮积症 I型 (MPS I)是由的溶酶体酶缺乏α（一种 遗传代谢性疾病 -iduronidase），这消除 艾杜糖醛酸 从的非还原性末端的硫酸皮肤素和 硫酸乙酰肝素 的逐步过程中的分解代谢的葡萄 糖 …