Literature DB >> 26667281

Axial myopathy: an overlooked feature of muscle diseases.

Nanna Witting1, Linda K Andersen2, John Vissing2.   

Abstract

Classically, myopathies are categorized according to limb or cranial nerve muscle affection, but with the growing use of magnetic resonance imaging it has become evident that many well-known myopathies have significant involvement of the axial musculature. New disease entities with selective axial muscle involvement have also been described recently, but overall the axial myopathy is unexplored. We performed a PubMed search using the search terms 'myopathy', 'paraspinal', 'axial' and 'erector'. Axial myopathy was defined as involvement of paraspinal musculature. We found evidence of axial musculature involvement in the majority of myopathies in which paraspinal musculature was examined. Even in diseases named after a certain pattern of non-axial muscle affection, such as facioscapulohumeral and limb girdle muscular dystrophies, affection of the axial musculature was often severe and early, compared to other muscle groups. Very sparse literature evaluating the validity of clinical assessment methods, electromyography, muscle biopsy and magnetic resonance imaging was identified and reference material is generally missing. This article provides an overview of the present knowledge on axial myopathy with the aim to increase awareness and spur interest among clinicians and researchers in the field.
© The Author (2015). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  axial; myopathy; paraspinal; rigid spine

Mesh:

Year:  2015        PMID: 26667281     DOI: 10.1093/brain/awv332

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  11 in total

1.  Chemotherapy dosing and toxicity in a patient with muscular dystrophy.

Authors:  Chris Lomma; David Ransom
Journal:  Cancer Rep (Hoboken)       Date:  2018-06-04

Review 2.  Pompe disease: what are we missing?

Authors:  Benedikt Schoser
Journal:  Ann Transl Med       Date:  2019-07

Review 3.  MR imaging of inherited myopathies: a review and proposal of imaging algorithms.

Authors:  Laís Uyeda Aivazoglou; Julio Brandão Guimarães; Thomas M Link; Maria Alice Freitas Costa; Fabiano Nassar Cardoso; Bruno de Mattos Lombardi Badia; Igor Braga Farias; Wladimir Bocca Vieira de Rezende Pinto; Paulo Victor Sgobbi de Souza; Acary Souza Bulle Oliveira; Alzira Alves de Siqueira Carvalho; André Yui Aihara; Artur da Rocha Corrêa Fernandes
Journal:  Eur Radiol       Date:  2021-04-21       Impact factor: 5.315

4.  Muscle MRI in neutral lipid storage disease (NLSD).

Authors:  Matteo Garibaldi; Giorgio Tasca; Jordi Diaz-Manera; Pierfancesco Ottaviani; Francesco Laschena; Donatella Pantoli; Simonetta Gerevini; Chiara Fiorillo; Lorenzo Maggi; Elisabetta Tasca; Adele D'Amico; Olimpia Musumeci; Antonio Toscano; Claudio Bruno; Roberto Massa; Corrado Angelini; Enrico Bertini; Giovanni Antonini; Elena Maria Pennisi
Journal:  J Neurol       Date:  2017-05-13       Impact factor: 4.849

5.  Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study.

Authors:  Rianne J M Goselink; Tim H A Schreuder; Nens van Alfen; Imelda J M de Groot; Merel Jansen; Richard J L F Lemmers; Patrick J van der Vliet; Nienke van der Stoep; Thomas Theelen; Nicol C Voermans; Silvère M van der Maarel; Baziel G M van Engelen; Corrie E Erasmus
Journal:  Ann Neurol       Date:  2018-10-16       Impact factor: 10.422

6.  Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy.

Authors:  Markus T Sainio; Salla Välipakka; Bruno Rinaldi; Helena Lapatto; Anders Paetau; Simo Ojanen; Virginia Brilhante; Manu Jokela; Sanna Huovinen; Mari Auranen; Johanna Palmio; Sylvie Friant; Emil Ylikallio; Bjarne Udd; Henna Tyynismaa
Journal:  J Neurol       Date:  2018-12-04       Impact factor: 4.849

7.  Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report.

Authors:  Matthias Türk; Armin M Nagel; Frank Roemer; Ursula Schlötzer-Schrehardt; Christian T Thiel; Martin Winterholler; Rolf Schröder
Journal:  BMC Musculoskelet Disord       Date:  2019-11-20       Impact factor: 2.362

8.  Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.

Authors:  Giulia Ricci; Fabiano Mele; Monica Govi; Lucia Ruggiero; Francesco Sera; Liliana Vercelli; Cinzia Bettio; Lucio Santoro; Tiziana Mongini; Luisa Villa; Maurizio Moggio; Massimiliano Filosto; Marina Scarlato; Stefano C Previtali; Silvia Maria Tripodi; Elena Pegoraro; Roberta Telese; Antonio Di Muzio; Carmelo Rodolico; Elisabetta Bucci; Giovanni Antonini; Maria Grazia D'Angelo; Angela Berardinelli; Lorenzo Maggi; Rachele Piras; Maria Antonietta Maioli; Gabriele Siciliano; Giuliano Tomelleri; Corrado Angelini; Rossella Tupler
Journal:  Sci Rep       Date:  2020-12-10       Impact factor: 4.379

9.  Patients With Becker Muscular Dystrophy Have Severe Paraspinal Muscle Involvement.

Authors:  Aisha M Sheikh; Karen Rudolf; Josefine de Stricker Borch; Tahmina Khawajazada; Nanna Witting; John Vissing
Journal:  Front Neurol       Date:  2021-05-21       Impact factor: 4.003

Review 10.  Pathophysiological Concepts and Treatment of Camptocormia.

Authors:  N G Margraf; A Wrede; G Deuschl; W J Schulz-Schaeffer
Journal:  J Parkinsons Dis       Date:  2016-06-16       Impact factor: 5.568

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.