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The Etiology of Primary Hyperhidrosis: A Systematic Review

机译:原发性患病的病因:系统审查

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Abstract Purpose Primary hyperhidrosis is a pathological disorder of unknown etiology, affecting 0.6-5% of the population, and causing severe functional and social handicaps. As the etiology is unknown, it is not possible to treat the root cause. Recently some differences between affected and non-affected people have been reported. The aim of this review is to summarize these new etiological data. Methods Search of the literature was performed in the PubMed/Medline Database and pertinent articles were retrieved and reviewed. Additional publications were obtained from the references of these articles. Results Some anatomical and pathophysiological characteristics (as well as enzymatic, metabolic, and neurological dysfunctions) have been observed in hyperhidrotic subjects; three main possible etiological factors predominate. A familial trait seems to exist, and genetic loci associated with hyperhidrosis have been identified. Histological differences were observed in sympathetic ganglia of hyperhidrotic subjects: the ganglia were larger and contained a higher number of ganglion cells. A higher expression of acetylcholine and alpha-7 neuronal nicotinic receptor subunit in the sympathetic ganglia of patients with hyperhidrosis has been reported. Conclusions Despite these accumulated data, the etiology of primary hyperhidrosis remains obscure. Nevertheless, three main lines for future research seem to be delineated: genetics, histological observations, and enzymatic studies. ]]>
机译:摘要目的原发性血清病因是未知病因的病理障碍,影响人口的0.6-5%,并造成严重的功能和社交障碍。由于病因未知,因此不可能治疗根本原因。最近报告了受影响和非受影响的人之间的一些差异。本综述的目的是总结这些新的病因数据。方法搜索文献中的文献,并检索和审查相关文章。从这些文章的参考文献中获得了其他出版物。结果在综合征受试者中观察到一些解剖学和病理生理学特征(以及酶促,代谢和神经功能障碍);三个主要可能的病因因素占主导地位。似乎存在家族性状,已经确定了与高脂症相关的遗传基因座。观察到组织学差异在综合征主题的同情神经节中:神经节较大,含有较高数量的神经节细胞。据报道,乙酰胆碱和α-7神经元烟碱受体亚基的表达较高。结论尽管存在这些累计数据,但原发性患病的病因仍然模糊不清。尽管如此,未来研究的三条主要线条似乎是划定的:遗传学,组织学观察和酶研究。 ]]>

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