Literature DB >> 25088881

A family with distal hereditary motor neuropathy and a K141Q mutation of small heat shock protein HSPB1.

Kengo Maeda1, Ryo Idehara, Akihiro Hashiguchi, Hiroshi Takashima.   

Abstract

We herein describe a Japanese family with distal hereditary motor neuropathy carrying a K141Q mutation of small heat shock protein HSPB1. Two patients among them had late onset disease (older than 50 years). The muscles of the distal legs were weak and atrophic. Sensory and autonomic dysfunction were not seen. Even eight years after onset, one patient could still walk without support. A nerve conduction study revealed axonal degeneration of the motor nerves of the legs. A heterozygous K141Q mutation was detected in the affected patients. The late onset and mild clinical phenotype might reflect the mild biochemical alteration of HSP27 induced by the K141Q mutation.

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Year:  2014        PMID: 25088881     DOI: 10.2169/internalmedicine.53.2843

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  11 in total

1.  Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2.

Authors:  Jun-Hui Yuan; Akihiro Hashiguchi; Yuji Okamoto; Akiko Yoshimura; Masahiro Ando; Kazutaka Shiomi; Kayoko Saito; Makoto Takahashi; Keiko Ichinose; Takuma Ohmichi; Kazushi Ichikawa; Adachi Tadashi; Hiroshi Takigawa; Hidehiro Shibayama; Hiroshi Takashima
Journal:  J Hum Genet       Date:  2018-01-10       Impact factor: 3.172

2.  Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatments.

Authors:  Takaki Taniguchi; Masahiro Ando; Yuji Okamoto; Akiko Yoshimura; Yujiro Higuchi; Akihiro Hashiguchi; Nozomu Matsuda; Mamoru Yamamoto; Eisuke Dohi; Makoto Takahashi; Masanao Yoshino; Taichi Nomura; Masaaki Matsushima; Ichiro Yabe; Yui Sanpei; Hiroyuki Ishiura; Jun Mitsui; Masanori Nakagawa; Shoji Tsuji; Hiroshi Takashima
Journal:  J Hum Genet       Date:  2022-01-14       Impact factor: 3.172

3.  Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes.

Authors:  Yu Hiramatsu; Yuji Okamoto; Akiko Yoshimura; Jun-Hui Yuan; Masahiro Ando; Yujiro Higuchi; Akihiro Hashiguchi; Eiji Matsuura; Fumihito Nozaki; Tomohiro Kumada; Kei Murayama; Mikiya Suzuki; Yuki Yamamoto; Naoko Matsui; Yoshimichi Miyazaki; Masamitsu Yamaguchi; Youji Suzuki; Jun Mitsui; Hiroyuki Ishiura; Masaki Tanaka; Shinichi Morishita; Ichizo Nishino; Shoji Tsuji; Hiroshi Takashima
Journal:  J Neurol       Date:  2022-03-02       Impact factor: 6.682

Review 4.  Chaperonopathies: Spotlight on Hereditary Motor Neuropathies.

Authors:  Vincenzo Lupo; Carmen Aguado; Erwin Knecht; Carmen Espinós
Journal:  Front Mol Biosci       Date:  2016-12-14

5.  Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study.

Authors:  Masahiro Ando; Akihiro Hashiguchi; Yuji Okamoto; Akiko Yoshimura; Yu Hiramatsu; Junhui Yuan; Yujiro Higuchi; Jun Mitsui; Hiroyuki Ishiura; Ayako Umemura; Koichi Maruyama; Takeshi Matsushige; Shinichi Morishita; Masanori Nakagawa; Shoji Tsuji; Hiroshi Takashima
Journal:  J Peripher Nerv Syst       Date:  2017-07-30       Impact factor: 3.494

Review 6.  Small heat shock proteins in neurodegenerative diseases.

Authors:  Leen Vendredy; Elias Adriaenssens; Vincent Timmerman
Journal:  Cell Stress Chaperones       Date:  2020-04-22       Impact factor: 3.667

7.  Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.

Authors:  Yujiro Higuchi; Akihiro Hashiguchi; Junhui Yuan; Akiko Yoshimura; Jun Mitsui; Hiroyuki Ishiura; Masaki Tanaka; Satoshi Ishihara; Hajime Tanabe; Satoshi Nozuma; Yuji Okamoto; Eiji Matsuura; Ryuichi Ohkubo; Saeko Inamizu; Wataru Shiraishi; Ryo Yamasaki; Yasumasa Ohyagi; Jun-ichi Kira; Yasushi Oya; Hayato Yabe; Noriko Nishikawa; Shinsuke Tobisawa; Nozomu Matsuda; Masayuki Masuda; Chiharu Kugimoto; Kazuhiro Fukushima; Satoshi Yano; Jun Yoshimura; Koichiro Doi; Masanori Nakagawa; Shinichi Morishita; Shoji Tsuji; Hiroshi Takashima
Journal:  Ann Neurol       Date:  2016-03-17       Impact factor: 10.422

8.  Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.

Authors:  Hajime Tanabe; Yujiro Higuchi; Jun-Hui Yuan; Akihiro Hashiguchi; Akiko Yoshimura; Satoshi Ishihara; Satoshi Nozuma; Yuji Okamoto; Eiji Matsuura; Hiroyuki Ishiura; Jun Mitsui; Ryotaro Takashima; Norito Kokubun; Kengo Maeda; Yuri Asano; Yoko Sunami; Yu Kono; Yasunori Ishigaki; Shosaburo Yanamoto; Jiro Fukae; Hiroshi Kida; Mitsuya Morita; Shoji Tsuji; Hiroshi Takashima
Journal:  J Peripher Nerv Syst       Date:  2018-02-14       Impact factor: 3.494

9.  Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan.

Authors:  Akiko Yoshimura; Jun-Hui Yuan; Akihiro Hashiguchi; Masahiro Ando; Yujiro Higuchi; Tomonori Nakamura; Yuji Okamoto; Masanori Nakagawa; Hiroshi Takashima
Journal:  J Neurol Neurosurg Psychiatry       Date:  2018-09-26       Impact factor: 10.154

10.  Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan.

Authors:  Takaki Taniguchi; Masahiro Ando; Yuji Okamoto; Akiko Yoshimura; Yujiro Higuchi; Akihiro Hashiguchi; Kensuke Shiga; Arisa Hayashida; Taku Hatano; Hiroyuki Ishiura; Jun Mitsui; Nobutaka Hattori; Toshiki Mizuno; Masanori Nakagawa; Shoji Tsuji; Hiroshi Takashima
Journal:  Clin Genet       Date:  2020-11-27       Impact factor: 4.438

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