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亨特综合征。幼儿的超微结构特征。

Hunter' syndrome. Ultrastructural features in young children.

作者信息

Murphy J V, Hodach A E, Gilbert E F, Deanching M, Matalon R

出版信息

Arch Pathol Lab Med. 1983 Sep;107(9):495-9.

PMID:6309115
Abstract

Ultrastructural abnormalities in two stepbrothers with Hunter's syndrome, ages 1 and 4 years, were found in cortical neurons, neurons of the myenteric plexus, and skin. Inclusions containing little or no electron-dense material were noted in most tissues, and lamellar figures were restricted to cortical neurons and neurons of the myenteric plexus. These changes correlate with those described in tissues obtained at post mortem.

摘要

在两名分别为1岁和4岁的患有亨特综合征的继兄弟中,在皮质神经元、肌间神经丛神经元和皮肤中发现了超微结构异常。在大多数组织中都发现了含有少量或不含电子致密物质的包涵体,而板层结构则仅限于皮质神经元和肌间神经丛神经元。这些变化与死后获得的组织中所描述的变化相关。

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