Literature DB >> 29478600

The genetics of congenital myopathies.

Hernan D Gonorazky1, Carsten G Bönnemann2, James J Dowling3.   

Abstract

Congenital myopathies are a clinically and genetically heterogeneous group of conditions that most commonly present at or around the time of birth with hypotonia, muscle weakness, and (often) respiratory distress. Historically, this group of disorders has been subclassified based on muscle histopathologic characteristics. There has been an explosion of gene discovery, and there are now at least 32 different genetic causes of disease. With this increased understanding of the genetic basis of disease has come the knowledge that the mutations in congenital myopathy genes can present with a wide variety of clinical phenotypes and can result in a broad spectrum of histopathologic findings on muscle biopsy. In addition, mutations in several genes can share the same histopathologic features. The identification of new genes and interpretation of different pathomechanisms at a molecular level have helped us to understand the clinical and histopathologic similarities that this group of disorders share. In this review, we highlight the genetic understanding for each subtype, its pathogenesis, and the future key issues in congenital myopathies.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  animal; central core; centronuclear; congenital; genetics; human; model; mutation; myopathies; nemaline; structural

Mesh:

Substances:

Year:  2018        PMID: 29478600     DOI: 10.1016/B978-0-444-64076-5.00036-3

Source DB:  PubMed          Journal:  Handb Clin Neurol        ISSN: 0072-9752


  31 in total

1.  Value of structured reporting in neuromuscular disorders.

Authors:  Francesco Alessandrino; Lara Cristiano; Claudia Maria Cinnante; Tommaso Tartaglione; Simonetta Gerevini; Tommaso Verdolotti; Giovanna Stefania Colafati; Emanuele Ghione; Raimondo Vitale; Lorenzo Peverelli; Claudia Brogna; Angela Berardinelli; Maurizio Moggio; Eugenio M Mercuri; Anna Pichiecchio
Journal:  Radiol Med       Date:  2019-03-09       Impact factor: 3.469

2.  Mouse model of severe recessive RYR1-related myopathy.

Authors:  Stephanie Brennan; Maricela Garcia-Castañeda; Antonio Michelucci; Nesrin Sabha; Sundeep Malik; Linda Groom; Lan Wei LaPierre; James J Dowling; Robert T Dirksen
Journal:  Hum Mol Genet       Date:  2019-09-15       Impact factor: 6.150

3.  Dysregulation of NRAP degradation by KLHL41 contributes to pathophysiology in nemaline myopathy.

Authors:  Caroline Jirka; Jasmine H Pak; Claire A Grosgogeat; Michael Mario Marchetii; Vandana A Gupta
Journal:  Hum Mol Genet       Date:  2019-08-01       Impact factor: 6.150

4.  A mutation in MTM1 causes X-Linked myotubular myopathy in Boykin spaniels.

Authors:  Natasha J Olby; Steven Friedenberg; Kathryn Meurs; Dylan DeProspero; Julien Guevar; Jeanie Lau; Oriana Yost; Ling T Guo; G Diane Shelton
Journal:  Neuromuscul Disord       Date:  2020-03-05       Impact factor: 4.296

5.  Multi-omics comparisons of different forms of centronuclear myopathies and the effects of several therapeutic strategies.

Authors:  Sarah Djeddi; David Reiss; Alexia Menuet; Sébastien Freismuth; Juliana de Carvalho Neves; Sarah Djerroud; Xènia Massana-Muñoz; Anne-Sophie Sosson; Christine Kretz; Wolfgang Raffelsberger; Céline Keime; Olivier M Dorchies; Julie Thompson; Jocelyn Laporte
Journal:  Mol Ther       Date:  2021-05-01       Impact factor: 12.910

Review 6.  Ryanodine Receptor 1-Related Myopathies: Diagnostic and Therapeutic Approaches.

Authors:  Tokunbor A Lawal; Joshua J Todd; Katherine G Meilleur
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

Review 7.  Molecular and cellular basis of genetically inherited skeletal muscle disorders.

Authors:  James J Dowling; Conrad C Weihl; Melissa J Spencer
Journal:  Nat Rev Mol Cell Biol       Date:  2021-07-13       Impact factor: 94.444

8.  Mice with muscle-specific deletion of Bin1 recapitulate centronuclear myopathy and acute downregulation of dynamin 2 improves their phenotypes.

Authors:  Roberto Silva-Rojas; Vasugi Nattarayan; Francisco Jaque-Fernandez; Raquel Gomez-Oca; Alexia Menuet; David Reiss; Marie Goret; Nadia Messaddeq; Valentina M Lionello; Christine Kretz; Belinda S Cowling; Vincent Jacquemond; Jocelyn Laporte
Journal:  Mol Ther       Date:  2021-08-08       Impact factor: 11.454

Review 9.  Inherited Defects of the ASC-1 Complex in Congenital Neuromuscular Diseases.

Authors:  Justine Meunier; Rocio-Nur Villar-Quiles; Isabelle Duband-Goulet; Ana Ferreiro
Journal:  Int J Mol Sci       Date:  2021-06-03       Impact factor: 5.923

10.  Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism.

Authors:  Johan Lindqvist; Weikang Ma; Frank Li; Yaeren Hernandez; Justin Kolb; Balazs Kiss; Paola Tonino; Robbert van der Pijl; Esmat Karimi; Henry Gong; Josh Strom; Zaynab Hourani; John E Smith; Coen Ottenheijm; Thomas Irving; Henk Granzier
Journal:  Nat Commun       Date:  2020-06-01       Impact factor: 14.919

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