Literature DB >> 17764830

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

Kengo Maeda1, Makoto Sugiura, Hiroko Kato, Mitsuru Sanada, Hiromichi Kawai, Hitoshi Yasuda.   

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.

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Year:  2007        PMID: 17764830     DOI: 10.1016/j.clineuro.2007.07.015

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  4 in total

1.  The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patients.

Authors:  Natsumi Fujisaki; Shugo Suwazono; Masahito Suehara; Ryo Nakachi; Miwako Kido; Yoshihisa Fujiwara; Saki Oshiro; Takashi Tokashiki; Hiroshi Takashima; Masanori Nakagawa
Journal:  Intractable Rare Dis Res       Date:  2018-02

2.  The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.

Authors:  Hiroyuki Ishiura; Wataru Sako; Mari Yoshida; Toshitaka Kawarai; Osamu Tanabe; Jun Goto; Yuji Takahashi; Hidetoshi Date; Jun Mitsui; Budrul Ahsan; Yaeko Ichikawa; Atsushi Iwata; Hiide Yoshino; Yuishin Izumi; Koji Fujita; Kouji Maeda; Satoshi Goto; Hidetaka Koizumi; Ryoma Morigaki; Masako Ikemura; Naoko Yamauchi; Shigeo Murayama; Garth A Nicholson; Hidefumi Ito; Gen Sobue; Masanori Nakagawa; Ryuji Kaji; Shoji Tsuji
Journal:  Am J Hum Genet       Date:  2012-08-10       Impact factor: 11.025

3.  Proteasome impairment in neural cells derived from HMSN-P patient iPSCs.

Authors:  Nagahisa Murakami; Keiko Imamura; Yuishin Izumi; Naohiro Egawa; Kayoko Tsukita; Takako Enami; Takuya Yamamoto; Toshitaka Kawarai; Ryuji Kaji; Haruhisa Inoue
Journal:  Mol Brain       Date:  2017-02-15       Impact factor: 4.041

Review 4.  Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies.

Authors:  Kristien Peeters; Teodora Chamova; Albena Jordanova
Journal:  Brain       Date:  2014-06-25       Impact factor: 13.501

  4 in total

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