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[门克斯卷发综合征:一例临床及病理病例报告,特别提及脑损伤中的胶质细胞变化]

[Menkes' kinky hair disease: a clinical and pathological case report with special reference to glial changes in the brain damage].

作者信息

Engel U, Ramaswamy A, Mennel H D, Wolf C, Dauner I

机构信息

Abteilung für Neuropathologie, Medizinisches Zentrum für Pathologie, Marburg, Deutschland.

出版信息

Zentralbl Pathol. 1994 Nov;140(4-5):383-90.

PMID:7826987
Abstract

Menkes' kinky hair disease (Kinky hair disease, trichopoliodystrophy) is a rare hereditary disease of copper metabolism. In this study we report about the case of a boy with a long course of disease who died at the age of 6. The last phase of the disease was characterized by an almost uncontrollable excitation stage and later by an apallic syndrome. Clinical course and autopsy result are presented here. The protracted course obviously led to unusual neuropathological changes. In addition to the known neuronal damages an excessive reactive gliosis could be found. The unusual neuropathological course of this gliosis perhaps allows the conclusion that apart from neuronal damages disturbances of copper metabolism have an influence on the glia.

摘要

门克斯卷发综合征(卷发综合征、毛发硫营养不良)是一种罕见的铜代谢遗传性疾病。在本研究中,我们报告了一例病程较长、6岁死亡的男孩病例。疾病的最后阶段以几乎无法控制的兴奋期为特征,随后发展为去大脑皮质综合征。本文介绍了临床病程和尸检结果。病程迁延显然导致了异常的神经病理学变化。除了已知的神经元损伤外,还发现了过度的反应性胶质增生。这种胶质增生异常的神经病理学过程或许可以得出这样的结论:除了神经元损伤外,铜代谢紊乱也会对神经胶质产生影响。

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