Literature DB >> 31060724

Myoimaging in Congenital Myopathies.

Robert-Yves Carlier1, Susana Quijano-Roy2.   

Abstract

There is a great clinical and genetic heterogeneity in congenital myopathies. Myo-MRI with pattern recognition has become a first-line complementary tool in clinical practice for this group of diseases. For diagnostic purposes, whole-body imaging techniques are preferred when involvement is axial or diffuse, as in most congenital myopathies, because of involvement of the tongue, masticator, neck or trunk muscles. Myo-MRI is widely used to identify abnormalities in muscle signal, volume or texture. Recognizable profiles or patterns have been identified in many of these genetic myopathies. The role of the radiologist is crucial in order to adapt the Myo-MRI protocols to the age of the patient and several clinical situations. Myo-MRI in children with congenital myopathies is a very demanding technique with a balance between acceptable time of examination and sufficient spatial resolution in order to detect subtle changes. Technical evolutions combining qualitative and quantitative analysis are useful to follow disease progression overtime. Outcome measures are expected to play a role in natural history description as well as in future therapeutic trials. Genetic diagnosis and interpretation of next generation sequencing results could be greatly influenced by statistical analysis with tools such as algorithms as well as graphical representations using heatmaps.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31060724     DOI: 10.1016/j.spen.2019.03.019

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  5 in total

Review 1.  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

2.  ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy.

Authors:  Rocío N Villar-Quiles; Fabio Catervi; Eva Cabet; Raul Juntas-Morales; Casie A Genetti; Teresa Gidaro; Asuman Koparir; Adnan Yüksel; Sandra Coppens; Nicolas Deconinck; Emma Pierce-Hoffman; Xavière Lornage; Julien Durigneux; Jocelyn Laporte; John Rendu; Norma B Romero; Alan H Beggs; Laurent Servais; Mireille Cossée; Montse Olivé; Johann Böhm; Isabelle Duband-Goulet; Ana Ferreiro
Journal:  Ann Neurol       Date:  2019-12-27       Impact factor: 10.422

Review 3.  Update on Congenital Myopathies in Adulthood.

Authors:  George Konstantinos Papadimas; Sophia Xirou; Evangelia Kararizou; Constantinos Papadopoulos
Journal:  Int J Mol Sci       Date:  2020-05-24       Impact factor: 5.923

4.  Natural history of a mouse model of X-linked myotubular myopathy.

Authors:  Ege Sarikaya; Nesrin Sabha; Jonathan Volpatti; Emanuela Pannia; Nika Maani; Hernan D Gonorazky; Alper Celik; Yijng Liang; Paula Onofre-Oliveira; James J Dowling
Journal:  Dis Model Mech       Date:  2022-07-25       Impact factor: 5.732

5.  Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials.

Authors:  Matteo Garibaldi; Tommaso Nicoletti; Elisabetta Bucci; Laura Fionda; Luca Leonardi; Stefania Morino; Laura Tufano; Girolamo Alfieri; Antonio Lauletta; Gioia Merlonghi; Alessia Perna; Salvatore Rossi; Enzo Ricci; Jorge Alonso Perez; Tommaso Tartaglione; Antonio Petrucci; Elena Maria Pennisi; Marco Salvetti; Gary Cutter; Jordi Díaz-Manera; Gabriella Silvestri; Giovanni Antonini
Journal:  Eur J Neurol       Date:  2021-12-06       Impact factor: 6.288

  5 in total

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