Literature DB >> 22392505

Congenital myopathies: an update.

Jessica R Nance1, James J Dowling, Elizabeth M Gibbs, Carsten G Bönnemann.   

Abstract

Congenital myopathy is a clinicopathological concept of characteristic histopathological findings on muscle biopsy in a patient with early-onset weakness. Three main categories are recognized within the classical congenital myopathies: nemaline myopathy, core myopathy, and centronuclear myopathy. Recent evidence of overlapping clinical and histological features between the classical forms and their different genetic entities suggests that there may be shared pathomechanisms between the congenital myopathies. Animal models, especially mouse and zebrafish, have been especially helpful in elucidating such pathomechanisms associated with the congenital myopathies and provide models in which future therapies can be investigated.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22392505      PMCID: PMC4491488          DOI: 10.1007/s11910-012-0255-x

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


  102 in total

1.  Central core disease of muscle: clinical, histochemical and electron microscopic studies of an affected mother and child.

Authors:  V Dubowitz; S Roy
Journal:  Brain       Date:  1970       Impact factor: 13.501

2.  Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy.

Authors:  Rachel D Susman; Susana Quijano-Roy; Nan Yang; Richard Webster; Nigel F Clarke; Jim Dowling; Marina Kennerson; Garth Nicholson; Valerie Biancalana; Biljana Ilkovski; Kevin M Flanigan; Susan Arbuckle; Chandra Malladi; Phillip Robinson; Steven Vucic; Michèle Mayer; Norma B Romero; Jon Andoni Urtizberea; Federico García-Bragado; Pascale Guicheney; Marc Bitoun; Robert-Yves Carlier; Kathryn N North
Journal:  Neuromuscul Disord       Date:  2010-03-12       Impact factor: 4.296

3.  Nebulin-deficient mice exhibit shorter thin filament lengths and reduced contractile function in skeletal muscle.

Authors:  Marie-Louise Bang; Xiaodong Li; Ryan Littlefield; Shannon Bremner; Andrea Thor; Kirk U Knowlton; Richard L Lieber; Ju Chen
Journal:  J Cell Biol       Date:  2006-06-12       Impact factor: 10.539

4.  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

5.  Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods.

Authors:  Elena Zvaritch; Natasha Kraeva; Eric Bombardier; Robert A McCloy; Frederic Depreux; Douglas Holmyard; Alexander Kraev; Christine E Seidman; J G Seidman; A Russell Tupling; David H MacLennan
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-03       Impact factor: 11.205

6.  "Necklace" fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy.

Authors:  Jorge A Bevilacqua; Marc Bitoun; Valérie Biancalana; Anders Oldfors; Gisela Stoltenburg; Kristl G Claeys; Emmanuelle Lacène; Guy Brochier; Linda Manéré; Pascal Laforêt; Bruno Eymard; Pascale Guicheney; Michel Fardeau; Norma Beatriz Romero
Journal:  Acta Neuropathol       Date:  2008-12-16       Impact factor: 17.088

7.  Dietary L-tyrosine supplementation in nemaline myopathy.

Authors:  Monique M Ryan; Catherine Sy; Sian Rudge; Carolyn Ellaway; David Ketteridge; Laurence G Roddick; Susan T Iannaccone; Andrew J Kornberg; Kathryn N North
Journal:  J Child Neurol       Date:  2007-12-13       Impact factor: 1.987

8.  X-inactivation patterns in carriers of X-linked myotubular myopathy.

Authors:  M Kristiansen; G P Knudsen; S M Tanner; M McEntagart; H Jungbluth; F Muntoni; C Sewry; S Gallati; K H Ørstavik; C Wallgren-Pettersson
Journal:  Neuromuscul Disord       Date:  2003-08       Impact factor: 4.296

9.  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

Review 10.  Centronuclear (myotubular) myopathy.

Authors:  Heinz Jungbluth; Carina Wallgren-Pettersson; Jocelyn Laporte
Journal:  Orphanet J Rare Dis       Date:  2008-09-25       Impact factor: 4.123

View more
  51 in total

1.  Analysis of embryonic and larval zebrafish skeletal myofibers from dissociated preparations.

Authors:  Eric J Horstick; Elizabeth M Gibbs; Xingli Li; Ann E Davidson; James J Dowling
Journal:  J Vis Exp       Date:  2013-11-13       Impact factor: 1.355

2.  Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A.

Authors:  Sandra Mercier; Xavière Lornage; Edoardo Malfatti; Pascale Marcorelles; Franck Letournel; Cécile Boscher; Gaëlle Caillaux; Armelle Magot; Johann Böhm; Anne Boland; Jean-François Deleuze; Norma Romero; Yann Péréon; Jocelyn Laporte
Journal:  Neurology       Date:  2016-12-21       Impact factor: 9.910

3.  Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores.

Authors:  Karen Majczenko; Ann E Davidson; Sandra Camelo-Piragua; Pankaj B Agrawal; Richard A Manfready; Xingli Li; Sucheta Joshi; Jishu Xu; Weiping Peng; Alan H Beggs; Jun Z Li; Margit Burmeister; James J Dowling
Journal:  Am J Hum Genet       Date:  2012-07-19       Impact factor: 11.025

4.  Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization.

Authors:  Gina L O'Grady; Heather A Best; Tamar E Sztal; Vanessa Schartner; Myriam Sanjuan-Vazquez; Sandra Donkervoort; Osorio Abath Neto; Roger Bryan Sutton; Biljana Ilkovski; Norma Beatriz Romero; Tanya Stojkovic; Jahannaz Dastgir; Leigh B Waddell; Anne Boland; Ying Hu; Caitlin Williams; Avnika A Ruparelia; Thierry Maisonobe; Anthony J Peduto; Stephen W Reddel; Monkol Lek; Taru Tukiainen; Beryl B Cummings; Himanshu Joshi; Juliette Nectoux; Susan Brammah; Jean-François Deleuze; Viola Oorschot Ing; Georg Ramm; Didem Ardicli; Kristen J Nowak; Beril Talim; Haluk Topaloglu; Nigel G Laing; Kathryn N North; Daniel G MacArthur; Sylvie Friant; Nigel F Clarke; Robert J Bryson-Richardson; Carsten G Bönnemann; Jocelyn Laporte; Sandra T Cooper
Journal:  Am J Hum Genet       Date:  2016-10-13       Impact factor: 11.025

5.  Novel SPEG mutations in congenital myopathies: Genotype-phenotype correlations.

Authors:  Anita E Qualls; Sandra Donkervoort; Johanna C Herkert; Alissa M D'gama; Diana Bharucha-Goebel; James Collins; Katherine R Chao; A Reghan Foley; Mirthe H Schoots; Jan D H Jongbloed; Carsten G Bönnemann; Pankaj B Agrawal
Journal:  Muscle Nerve       Date:  2018-11-28       Impact factor: 3.217

Review 6.  Recent advances using zebrafish animal models for muscle disease drug discovery.

Authors:  Lisa Maves
Journal:  Expert Opin Drug Discov       Date:  2014-06-14       Impact factor: 6.098

7.  ACTN2 mutations cause "Multiple structured Core Disease" (MsCD).

Authors:  Xavière Lornage; Norma B Romero; Claire A Grosgogeat; Edoardo Malfatti; Sandra Donkervoort; Michael M Marchetti; Sarah B Neuhaus; A Reghan Foley; Clémence Labasse; Raphaël Schneider; Robert Y Carlier; Katherine R Chao; Livija Medne; Jean-François Deleuze; David Orlikowski; Carsten G Bönnemann; Vandana A Gupta; Michel Fardeau; Johann Böhm; Jocelyn Laporte
Journal:  Acta Neuropathol       Date:  2019-01-30       Impact factor: 17.088

8.  Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric Cores.

Authors:  Sandra Donkervoort; Carl E Kutzner; Ying Hu; Xavière Lornage; John Rendu; Tanya Stojkovic; Jonathan Baets; Sarah B Neuhaus; Jantima Tanboon; Reza Maroofian; Véronique Bolduc; Magdalena Mroczek; Stefan Conijn; Nancy L Kuntz; Ana Töpf; Soledad Monges; Fabiana Lubieniecki; Riley M McCarty; Katherine R Chao; Serena Governali; Johann Böhm; Kanokwan Boonyapisit; Edoardo Malfatti; Tumtip Sangruchi; Iren Horkayne-Szakaly; Carola Hedberg-Oldfors; Stephanie Efthymiou; Satoru Noguchi; Sarah Djeddi; Aritoshi Iida; Gabriella di Rosa; Chiara Fiorillo; Vincenzo Salpietro; Niklas Darin; Julien Fauré; Henry Houlden; Anders Oldfors; Ichizo Nishino; Willem de Ridder; Volker Straub; Wojciech Pokrzywa; Jocelyn Laporte; A Reghan Foley; Norma B Romero; Coen Ottenheijm; Thorsten Hoppe; Carsten G Bönnemann
Journal:  Am J Hum Genet       Date:  2020-11-19       Impact factor: 11.025

9.  KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy.

Authors:  Ankit Garg; Jason O'Rourke; Chengzu Long; Jonathan Doering; Gianina Ravenscroft; Svetlana Bezprozvannaya; Benjamin R Nelson; Nadine Beetz; Lin Li; She Chen; Nigel G Laing; Robert W Grange; Rhonda Bassel-Duby; Eric N Olson
Journal:  J Clin Invest       Date:  2014-06-24       Impact factor: 14.808

10.  Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database.

Authors:  Jorge Oliveira; Márcia E Oliveira; Wolfram Kress; Ricardo Taipa; Manuel Melo Pires; Pascale Hilbert; Peter Baxter; Manuela Santos; Henk Buermans; Johan T den Dunnen; Rosário Santos
Journal:  Eur J Hum Genet       Date:  2012-09-12       Impact factor: 4.246

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.