Suppr超能文献

门克斯综合征临床表型的变异性。

Variability in clinical expression of Menkes syndrome.

作者信息

Gerdes A M, Tønnesen T, Pergament E, Sander C, Baerlocher K E, Wartha R, Güttler F, Horn N

机构信息

John F. Kennedy Institute, Glostrup, Denmark.

出版信息

Eur J Pediatr. 1988 Nov;148(2):132-5. doi: 10.1007/BF00445920.

Abstract

Six patients with Menkes syndrome are described, who differ from patients with the classical form of Menkes syndrome because of their longer survival; some of them also exhibited a milder manifestation of symptoms. Based on the present data and a summary of seven case reports describing Menkes patients with long survival, it may be possible to divide these patients into two subgroups: one group of severely affected patients with long survival and another group of very mildly affected patients with late onset of symptoms. Perhaps only the latter represents a true subgroup of Menkes syndrome. The possible benefits of copper therapy are discussed.

摘要

本文描述了6例门克斯综合征患者,他们与经典型门克斯综合征患者不同,生存期更长;其中一些患者症状表现也较轻。根据现有数据以及7例描述生存期长的门克斯综合征患者的病例报告总结,可能可以将这些患者分为两个亚组:一组是病情严重但生存期长的患者,另一组是症状出现较晚且病情非常轻微的患者。也许只有后者才是真正的门克斯综合征亚组。文中还讨论了铜疗法可能带来的益处。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验