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早发性青少年型巴滕病——一种与其他形式的巴滕病不同的可识别亚组。对5例患者的分析。

Early-juvenile Batten's disease--a recognisable sub-group distinct from other forms of Batten's disease. Analysis of 5 patients.

作者信息

Lake B D, Cavanagh N P

出版信息

J Neurol Sci. 1978 Apr;36(2):265-71. doi: 10.1016/0022-510x(78)90087-4.

Abstract

In most cases where rectal biopsy is performed to diagnose Batten's disease, there is good correlation between biopsy appearance, age of onset, clinical course and electrophysiological parameters. As a result 3 forms of the disease have been recognised; infantile, late infantile and juvenile. In a review of rectal biopsy in Batten's disease at the Hospital for Sick Children, Great Ormond Street, we have studied the few cases in which no such correlation appeared to exist. In 5 the features are sufficiently similar to suggest a further recognisable sub-group which could be descriptively called "early juvenile". The clinical course, electrophysiological features and the absence of vacuolated lymphocytes in this subgroup are as found in the late infantile form, whereas the biopsy findings are identical to those of the juvenile form. By analogy with some of the mucopolysaccharidoses we speculate that the genes of the late infantile and juvenile forms of Batten's disease are allelic and that the "early juvenile" sub-group is a genetic compound presenting as an intermediate phenotype.

摘要

在大多数通过直肠活检来诊断巴滕病的病例中,活检表现、发病年龄、临床病程和电生理参数之间存在良好的相关性。因此,该疾病已被确认有3种类型:婴儿型、晚婴儿型和青少年型。在对大奥蒙德街儿童医院巴滕病直肠活检的回顾中,我们研究了少数似乎不存在这种相关性的病例。在5例中,其特征非常相似,提示可能存在一个可进一步识别的亚组,可描述为“早青少年型”。该亚组的临床病程、电生理特征以及无空泡淋巴细胞的情况与晚婴儿型相同,而活检结果与青少年型相同。类比某些黏多糖贮积症,我们推测巴滕病晚婴儿型和青少年型的基因是等位基因,“早青少年”亚组是一种表现为中间表型的遗传复合物。

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