Literature DB >> 18367042

Congenital myopathies.

Adele D'Amico1, Enrico Bertini.   

Abstract

This review focuses on congenital myopathies, a distinct but markedly heterogeneous group of muscle disorders that present with muscle weakness and typically appear at birth or in infancy. These myopathies have characteristic histopathologic abnormalities on muscle biopsy, allowing a preliminary morphologic classification. Advances in molecular genetics have allowed a more rational classification of these disorders and have reshuffled taxonomy for some of these conditions. Here, we focus on recent research advances in specific congenital myopathies, including nemaline myopathy, myotubular myopathy, centronuclear myopathy, central core myopathy, multi-minicore myopathy, congenital fiber-type disproportion myopathy, and hyaline body myopathy. Scientific progress has not only elucidated the pathologic mechanisms of these disorders, but it has also provided the basis for therapeutic strategies.

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Year:  2008        PMID: 18367042     DOI: 10.1007/s11910-008-0012-3

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  49 in total

1.  118th ENMC International Workshop on Advances in Myotubular Myopathy. 26-28 September 2003, Naarden, The Netherlands. (5th Workshop of the International Consortium on Myotubular Myopathy).

Authors:  E Bertini; V Biancalana; A Bolino; A Buj Bello; M Clague; P Guicheney; H Jungbluth; W Kress; A Musaro'; H Nandurkar; L Pirola; N Romero; J Senderek; U Suter; C Sewry; H Tronchere; C Wallgren-Pettersson; M J Wishart; J Laporte
Journal:  Neuromuscul Disord       Date:  2004-06       Impact factor: 4.296

2.  Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2.

Authors:  Vilma-Lotta Lehtokari; Chantal Ceuterick-de Groote; Peter de Jonghe; Minttu Marttila; Nigel G Laing; Katarina Pelin; Carina Wallgren-Pettersson
Journal:  Neuromuscul Disord       Date:  2007-04-16       Impact factor: 4.296

3.  Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.

Authors:  Kati Donner; Miina Ollikainen; Maaret Ridanpää; Hans-Jürgen Christen; Hans H Goebel; Marianne de Visser; Katarina Pelin; Carina Wallgren-Pettersson
Journal:  Neuromuscul Disord       Date:  2002-02       Impact factor: 4.296

4.  A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathy.

Authors:  S R Hammans; D O Robinson; C Moutou; C R Kennedy; N R Dennis; P J Hughes; D W Ellison
Journal:  Neuromuscul Disord       Date:  2000-02       Impact factor: 4.296

5.  Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations.

Authors:  Heinz Jungbluth; Mark R Davis; Clemens Müller; Serena Counsell; Joanna Allsop; Arijit Chattopadhyay; Sonia Messina; Eugenio Mercuri; Nigel G Laing; Caroline A Sewry; Graeme Bydder; Francesco Muntoni
Journal:  Neuromuscul Disord       Date:  2004-12       Impact factor: 4.296

6.  Cardiac manifestations of congenital fiber-type disproportion myopathy.

Authors:  B L Banwell; L E Becker; V Jay; G P Taylor; J Vajsar
Journal:  J Child Neurol       Date:  1999-02       Impact factor: 1.987

7.  Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.

Authors:  H Jungbluth; H Zhou; L Hartley; B Halliger-Keller; S Messina; C Longman; M Brockington; S A Robb; V Straub; T Voit; M Swash; A Ferreiro; G Bydder; C A Sewry; C Müller; F Muntoni
Journal:  Neurology       Date:  2005-12-27       Impact factor: 9.910

8.  Myopathy mutations in alpha-skeletal-muscle actin cause a range of molecular defects.

Authors:  Céline F Costa; Heidi Rommelaere; Davy Waterschoot; Kamaljit K Sethi; Kristen J Nowak; Nigel G Laing; Christophe Ampe; Laura M Machesky
Journal:  J Cell Sci       Date:  2004-07-01       Impact factor: 5.285

9.  Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy.

Authors:  Christopher R Pierson; Pankaj B Agrawal; Jessica Blasko; Alan H Beggs
Journal:  Neuromuscul Disord       Date:  2007-05-29       Impact factor: 4.296

10.  Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype.

Authors:  Valérie Biancalana; Olivier Caron; Sabina Gallati; Frank Baas; Wolfram Kress; Giuseppe Novelli; Maria Rosaria D'Apice; Clotilde Lagier-Tourenne; Anna Buj-Bello; Norma B Romero; Jean-Louis Mandel
Journal:  Hum Genet       Date:  2002-11-28       Impact factor: 4.132

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  9 in total

1.  Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disorders.

Authors:  Yuri Kitamura; Eri Kondo; Mari Urano; Ryoko Aoki; Kayoko Saito
Journal:  J Hum Genet       Date:  2016-06-30       Impact factor: 3.172

Review 2.  Clinical approach to the diagnostic evaluation of hereditary and acquired neuromuscular diseases.

Authors:  Craig M McDonald
Journal:  Phys Med Rehabil Clin N Am       Date:  2012-08       Impact factor: 1.784

3.  Extradenticle and homothorax control adult muscle fiber identity in Drosophila.

Authors:  Anton L Bryantsev; Sandy Duong; Tonya M Brunetti; Maria B Chechenova; TyAnna L Lovato; Cloyce Nelson; Elizabeth Shaw; Juli D Uhl; Brian Gebelein; Richard M Cripps
Journal:  Dev Cell       Date:  2012-09-11       Impact factor: 12.270

4.  Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos.

Authors:  Christelle Etard; Urmas Roostalu; Uwe Strähle
Journal:  J Cell Biol       Date:  2010-05-03       Impact factor: 10.539

5.  Myogenesis in Drosophila melanogaster: Dissection of Distinct Muscle Types for Molecular Analysis.

Authors:  Anton L Bryantsev; Lizzet Castillo; Sandy T Oas; Maria B Chechenova; Tracy E Dohn; TyAnna L Lovato
Journal:  Methods Mol Biol       Date:  2019

Review 6.  History and development of staining methods for skeletal muscle fiber types.

Authors:  Shoko Sawano; Wataru Mizunoya
Journal:  Histol Histopathol       Date:  2022-01-19       Impact factor: 2.130

7.  A One-Step Immunostaining Method to Visualize Rodent Muscle Fiber Type within a Single Specimen.

Authors:  Shoko Sawano; Yusuke Komiya; Riho Ichitsubo; Yasuyuki Ohkawa; Mako Nakamura; Ryuichi Tatsumi; Yoshihide Ikeuchi; Wataru Mizunoya
Journal:  PLoS One       Date:  2016-11-04       Impact factor: 3.240

Review 8.  Ryanodine receptor 1-related disorders: an historical perspective and proposal for a unified nomenclature.

Authors:  Tokunbor A Lawal; Joshua J Todd; Jessica W Witherspoon; Carsten G Bönnemann; James J Dowling; Susan L Hamilton; Katherine G Meilleur; Robert T Dirksen
Journal:  Skelet Muscle       Date:  2020-11-16       Impact factor: 4.912

9.  Novel Variants in Individuals with RYR1-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings.

Authors:  Joshua J Todd; Muslima S Razaqyar; Jessica W Witherspoon; Tokunbor A Lawal; Ami Mankodi; Irene C Chrismer; Carolyn Allen; Mary D Meyer; Anna Kuo; Monique S Shelton; Kim Amburgey; Dmitriy Niyazov; Pierre Fequiere; Carsten G Bönnemann; James J Dowling; Katherine G Meilleur
Journal:  Front Neurol       Date:  2018-03-05       Impact factor: 4.003

  9 in total

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