粘多糖病VII (Sly综合征)的诊断和新兴治疗策略。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2022-01-01 DOI:10.2147/TCRM.S351300
Fabiano de Oliveira Poswar, Johanna Henriques Nehm, Francyne Kubaski, Edina Poletto, Roberto Giugliani
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引用次数: 4

摘要

粘多糖病VII (MPS VII, Sly综合征)是一种由酶β-葡萄糖醛酸酶(GUS)缺乏引起的超罕见溶酶体疾病。该诊断是基于许多其他MPS类型的常见症状,并通过生化和分子研究得到证实。除了支持治疗,目前和新兴的治疗方法包括酶替代治疗、造血干细胞移植和基因治疗。本文综述了MPS VII的临床表现、诊断和新兴治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Diagnosis and Emerging Treatment Strategies for Mucopolysaccharidosis VII (Sly Syndrome).

Mucopolysaccharidosis VII (MPS VII, Sly syndrome) is an ultra-rare lysosomal disease caused by a deficiency of the enzyme β-glucuronidase (GUS). The diagnosis is suspected based on a range of symptoms that are common to many other MPS types, and it is confirmed through biochemical and molecular studies. Besides supportive treatment, current and emerging treatments include enzyme replacement therapy, hematopoietic stem cell transplantation, and gene therapy. This review summarizes the clinical manifestations, diagnosis, and emerging treatments for MPS VII.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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