Clinical and imaging hallmarks of the MYH7‐related myopathy with severe axial involvement. Issue 2 (14th May 2018)

• Record Type: Journal Article
• Authors: Dabaj, Ivana; Carlier, Robert Y; Gómez‐Andrés, David; Neto, Osório Abath; Bertini, Enrico; D'amico, Adele; Fattori, Fabiana; PéRéon, Yann; Castiglioni, Claudia; Rodillo, Eliana; Catteruccia, Michela; Guimarães, júlio Brandão; Oliveira, Acary Souza Bulle; Reed, Umbertina Conti; Mesrob, Lilia; Lechner, Doris; Boland, Anne; Deleuze, Jean‐François; Malfatti, Edoardo; Bonnemann, Carsten; Laporte, Jocelyn; Romero, Norma; Felter, Adrien; Quijano‐Roy, Susana; Moreno, Cristiane Araújo Martins; Zanoteli, Edmar
• Is Part Of: Muscle & nerve. Volume 58:Issue 2(2018)
• Page Start: 224
• Page End: 234
• Publication Date: 2018-05-14
• Subjects: foot drop -- heatmap -- LMNA -- muscle imaging -- MYH7 -- rigid spine -- SEPN1; Neuromuscular diseases -- Periodicals; Muscles -- Periodicals; Nerves -- Periodicals; 616.74
• DOI: 10.1002/mus.26137
• Languages: English
• ISSNs: 0148-639X

Abstract

ABSTRACT: Introduction: MYH7 gene mutations are related to a heterogeneous group of skeletal and cardiac myopathies. Methods : We evaluated clinical and muscle MRI changes in patients with mutations in the rod domain of MYH7, including 1 with mosaicism and 3 with novel missense mutations. Results : Patients presented in childhood with a distal and axial phenotype. Biopsy findings were variable. Half of the cases displaying some type of core pathology, including minicores and eccentric cores. Most patients demonstrated internal bands of infiltration ("inverted‐collagen‐VI sign") in multiple muscles, particularly the soleus, and prominent atrophy and fatty infiltration of the tongue and the paraspinal, gluteus minimus, sartorius, gracilis, tibialis anterior, and extensor digitorum longus muscles. Discussion : Muscle imaging findings in patients with axial involvement provide significant clues permitting the distinction between MYH7 ‐related myopathies and other axial myopathies such as those related to SEPN1 and LMNA genes. Muscle Nerve 58 : 224–234, 2018