Suppr超能文献

X连锁隐性延髓脊髓神经元病

X-linked recessive bulbospinal neuronopathy.

作者信息

Phanthumchinda K

机构信息

Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 1992 Jun;75(6):369-73.

PMID:1487685
Abstract

The first case of X-linked recessive bulbospinal neuronopathy in a Thai family is described. Clinical features of this entity were discussed. Although two members of this family had classical features of X-linked recessive bulbospinal neuronopathy, there were some differences in distribution of weakness among the affected members. This variation among the members of the affected family was firstly described. The clinical features of this disease especially the associated gynecomastia and essential tremors are distinctive and it is possible to diagnose it even in a sporadic case. Although, the prominent feature of the disease is atrophy and fasciculation of muscles, this entity is not a pure anterior horn cell disorder and should be better classified as a multisystem disorder due to multiple organ involvement.

摘要

本文描述了一个泰国家庭中首例X连锁隐性延髓脊髓神经元病病例。讨论了该疾病实体的临床特征。尽管该家族的两名成员具有X连锁隐性延髓脊髓神经元病的典型特征,但受影响成员之间的肌无力分布存在一些差异。首次描述了受影响家族成员之间的这种变异。该疾病的临床特征,尤其是伴发的男性乳房发育和特发性震颤很独特,即使在散发病例中也有可能诊断出来。虽然该疾病的突出特征是肌肉萎缩和肌束震颤,但该疾病实体并非单纯的前角细胞疾病,由于多器官受累,应更好地归类为多系统疾病。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验