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婴儿期黏多糖贮积症VII型(β-葡萄糖醛酸酶缺乏症)的表现。

Presentation of mucopolysaccharidosis VII (beta-glucuronidase deficiency) in infancy.

作者信息

Hoyme H E, Jones K L, Higginbottom M C, O'Brien J S

出版信息

J Med Genet. 1981 Jun;18(3):237-9. doi: 10.1136/jmg.18.3.237.

Abstract

A child is presented with mucopolysaccharidosis VII (beta-glucuronidase deficiency), bringing to six the number of reported patients with the infantile onset form of this disorder. This patient exhibited the following features, previously unrecognised as part of this syndrome: presentation in the neonatal period, progressive joint contractures, and hydrocephalus. This child's course and data from published reports indicate that mucopolysaccharidosis VII, unlike the other known mucopolysaccharidoses, is clinically recognisable in the newborn period and is most likely to be associated with moderate mental deficiency which does not progress over time.

摘要

一名患有黏多糖贮积症VII型(β-葡萄糖醛酸酶缺乏症)的儿童,使该疾病婴儿期发病形式的报告患者数量增加到6例。该患者表现出以下特征,这些特征以前未被认为是该综合征的一部分:新生儿期发病、进行性关节挛缩和脑积水。该患儿的病程以及已发表报告中的数据表明,与其他已知的黏多糖贮积症不同,黏多糖贮积症VII型在新生儿期即可临床识别,并且最有可能与不会随时间进展的中度智力缺陷相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7131/1048714/c9a513d4b223/jmedgene00119-0079-a.jpg

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