Suppr超能文献

日裔巴西人中的遗传性运动和感觉神经病(近端显性型,HMSN-P)

Hereditary motor and sensory neuropathy (proximal dominant form, HMSN-P) among Brazilians of Japanese ancestry.

作者信息

Maeda Kengo, Sugiura Makoto, Kato Hiroko, Sanada Mitsuru, Kawai Hiromichi, Yasuda Hitoshi

机构信息

Division of Neurology, Department of Medicine, Shiga University of Medical Science, Seta-Tsukinowa, Otsu, Shiga 520-2192, Japan.

出版信息

Clin Neurol Neurosurg. 2007 Nov;109(9):830-2. doi: 10.1016/j.clineuro.2007.07.015. Epub 2007 Aug 30.

Abstract

Hereditary motor and sensory neuropathy (proximal dominant form, HMSN-P) has been reported exclusively from Okinawa Prefecture in Japan. We herein report three brothers with HMSN-P who are among Brazilians of Japanese ancestry. They showed the typical clinical manifestations and were compatible with HMSN-P. Okinawa Prefecture has been a site of emigration to other countries, mainly in South America, since 1908. Although this is the first reported familial case of HMSN-P occurring outside Japan, it is estimated that there are 19 or 20 individuals with HMSN-P among these emigrants. Since HMSN-P might be misdiagnosed as familial amyotrophic lateral sclerosis or spinal muscular atrophy, neurologists in countries where individuals of Okinawan extraction reside should be aware of this hereditary neuropathy. HMSN-P should no longer be regarded as an endemic condition limited to Okinawa.

摘要

遗传性运动和感觉神经病(近端优势型,HMSN-P)仅在日本冲绳县有报道。我们在此报告三名患有HMSN-P的兄弟,他们是日裔巴西人。他们表现出典型的临床表现,符合HMSN-P。自1908年以来,冲绳县一直是向其他国家,主要是南美洲移民的地区。虽然这是首次报道在日本以外发生的HMSN-P家族病例,但据估计,这些移民中有19或20人患有HMSN-P。由于HMSN-P可能被误诊为家族性肌萎缩侧索硬化症或脊髓性肌萎缩症,在有冲绳血统人群居住的国家,神经科医生应注意这种遗传性神经病。HMSN-P不应再被视为仅限于冲绳的地方病。

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