Literature DB >> 16817213

A case of dysferlinopathy presenting choreic movements.

Toshiaki Takahashi1, Masashi Aoki, Takashi Imai, Masaru Yoshioka, Hidehiko Konno, Shuichi Higano, Yoshiaki Onodera, Hiroshi Saito, Itaru Kimura, Yasuto Itoyama.   

Abstract

Mutations in the dysferlin gene cause limb-girdle muscular dystrophy type 2B (LGMD2B). The involvement of the central nervous system in dysferlinopathy has not been described. We describe the clinical features of a patient with LGMD2B associated with dysferlin mutations (homozygous G3370T) who presented progressive choreic movements. The patient had no evidence of other causes of chorea. It is suggested that the chorea may be associated with the altered expression of the brain isoform of dysferlin. (c) 2006 Movement Disorder Society.

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Year:  2006        PMID: 16817213     DOI: 10.1002/mds.21027

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  5 in total

1.  Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injury.

Authors:  Renzhi Han; Dimple Bansal; Katsuya Miyake; Viviane P Muniz; Robert M Weiss; Paul L McNeil; Kevin P Campbell
Journal:  J Clin Invest       Date:  2007-07       Impact factor: 14.808

2.  Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia.

Authors:  Norah Alharbi; Rawan Matar; Edward Cupler; Hindi Al-Hindi; Hatem Murad; Iftteah Alhomud; Dorota Monies; Ali Alshehri; Mossaed Alyahya; Brian Meyer; Saeed Bohlega
Journal:  Front Neurosci       Date:  2022-02-22       Impact factor: 4.677

3.  A Case of Obsessive-Compulsive Disorder Comorbid with Miyoshi Myopathy.

Authors:  Arpit Parmar; Rohit Verma
Journal:  Indian J Psychol Med       Date:  2018 Jan-Feb

4.  Progression to Loss of Ambulation Among Patients with Autosomal Recessive Limb-girdle Muscular Dystrophy: A Systematic Review.

Authors:  Ivana F Audhya; Antoinette Cheung; Shelagh M Szabo; Emma Flint; Conrad C Weihl; Katherine L Gooch
Journal:  J Neuromuscul Dis       Date:  2022

5.  Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B.

Authors:  Toshiaki Takahashi; Masashi Aoki; Naoki Suzuki; Maki Tateyama; Chikako Yaginuma; Hitomi Sato; Miho Hayasaka; Hitomi Sugawara; Mariko Ito; Emi Abe-Kondo; Naoko Shimakura; Tohru Ibi; Satoshi Kuru; Tadashi Wakayama; Gen Sobue; Naoki Fujii; Toshio Saito; Tsuyoshi Matsumura; Itaru Funakawa; Eiichiro Mukai; Toru Kawanami; Mitsuya Morita; Mineo Yamazaki; Takashi Hasegawa; Jun Shimizu; Shoji Tsuji; Shigeki Kuzuhara; Hiroyasu Tanaka; Masaru Yoshioka; Hidehiko Konno; Hiroshi Onodera; Yasuto Itoyama
Journal:  J Neurol Neurosurg Psychiatry       Date:  2012-12-15       Impact factor: 10.154

  5 in total

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