Literature DB >> 11805270

Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.

M Tateyama1, M Aoki, I Nishino, Y K Hayashi, S Sekiguchi, Y Shiga, T Takahashi, Y Onodera, K Haginoya, K Kobayashi, K Iinuma, I Nonaka, K Arahata, Y Itoyama, Y Itoyoma.   

Abstract

The authors describe a patient with sporadic distal myopathy associated with reduced caveolin-3 in muscle fibers in which the muscle atrophy was restricted to the small muscles of the hands and feet. Gene analysis disclosed a heterozygous 80 G-->A substitution in the caveolin-3 gene that was identical to that of reported cases of elevated serum creatine kinase. This patient further demonstrated possible clinical heterogeneity of myopathies with mutations in the caveolin-3 gene.

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Year:  2002        PMID: 11805270     DOI: 10.1212/wnl.58.2.323

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  13 in total

1.  Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

Authors:  Lisa B Cronk; Bin Ye; Toshihiko Kaku; David J Tester; Matteo Vatta; Jonathan C Makielski; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2006-12-06       Impact factor: 6.343

Review 2.  Caveolae, caveolins, and cavins: complex control of cellular signalling and inflammation.

Authors:  John H Chidlow; William C Sessa
Journal:  Cardiovasc Res       Date:  2010-03-03       Impact factor: 10.787

3.  Congenital generalized lipodystrophy, type 4 (CGL4) associated with myopathy due to novel PTRF mutations.

Authors:  Savitha Shastry; Mauricio R Delgado; Eray Dirik; Mehmet Turkmen; Anil K Agarwal; Abhimanyu Garg
Journal:  Am J Med Genet A       Date:  2010-09       Impact factor: 2.802

4.  Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).

Authors:  Christopher Meredith; Ralf Herrmann; Cheryl Parry; Khema Liyanage; Danielle E Dye; Hayley J Durling; Rachael M Duff; Kaye Beckman; Marianne de Visser; Maaike M van der Graaff; Peter Hedera; John K Fink; Elizabeth M Petty; Phillipa Lamont; Vicki Fabian; Leslie Bridges; Thomas Voit; Frank L Mastaglia; Nigel G Laing
Journal:  Am J Hum Genet       Date:  2004-08-20       Impact factor: 11.025

Review 5.  Distal myopathies.

Authors:  Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2014-05-15       Impact factor: 3.806

6.  Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.

Authors:  Jan Senderek; Sean M Garvey; Michael Krieger; Velina Guergueltcheva; Andoni Urtizberea; Andreas Roos; Miriam Elbracht; Claudia Stendel; Ivailo Tournev; Violeta Mihailova; Howard Feit; Jeff Tramonte; Peter Hedera; Kristy Crooks; Carsten Bergmann; Sabine Rudnik-Schöneborn; Klaus Zerres; Hanns Lochmüller; Eric Seboun; Joachim Weis; Jacques S Beckmann; Michael A Hauser; Charles E Jackson
Journal:  Am J Hum Genet       Date:  2009-04-02       Impact factor: 11.025

Review 7.  Caveolinopathies: from the biology of caveolin-3 to human diseases.

Authors:  Elisabetta Gazzerro; Federica Sotgia; Claudio Bruno; Michael P Lisanti; Carlo Minetti
Journal:  Eur J Hum Genet       Date:  2009-07-08       Impact factor: 4.246

8.  Phosphofructokinase muscle-specific isoform requires caveolin-3 expression for plasma membrane recruitment and caveolar targeting: implications for the pathogenesis of caveolin-related muscle diseases.

Authors:  Federica Sotgia; Gloria Bonuccelli; Carlo Minetti; Scott E Woodman; Franco Capozza; Robert G Kemp; Philipp E Scherer; Michael P Lisanti
Journal:  Am J Pathol       Date:  2003-12       Impact factor: 4.307

9.  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

10.  Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing.

Authors:  Rumiko Izumi; Tetsuya Niihori; Toshiaki Takahashi; Naoki Suzuki; Maki Tateyama; Chigusa Watanabe; Kazuma Sugie; Hirotaka Nakanishi; Gen Sobue; Masaaki Kato; Hitoshi Warita; Yoko Aoki; Masashi Aoki
Journal:  Neurol Genet       Date:  2015-12-10
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