Titre :

MYH7-related myopathies: clinical, myopathological and genotypic spectrum in a multicentre French cohort

Auteur(s) :

Bahout, M. [Auteur]
Severa, G. [Auteur]
Kamoun, E. [Auteur]
Bouhour, F. [Auteur]
Pegat, A. [Auteur]
Toutain, A. [Auteur]
Lagrange, E. [Auteur]
Duval, F. [Auteur]
Tard, Celine [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
De La Cruz, E. [Auteur]
Féasson, L. [Auteur]
Jacquin-Piques, A. [Auteur]
Richard, P. [Auteur]
Métay, C. [Auteur]
Cavalli, M. [Auteur]
Romero, N. B. [Auteur]
Evangelista, T. [Auteur]
Sole, G. [Auteur]
Carlier, R. Y. [Auteur]
Laforêt, P. [Auteur]
Acket, B. [Auteur]
Behin, A. [Auteur]
Fernández-Eulate, G. [Auteur]
Léonard-Louis, S. [Auteur]
Quijano-Roy, S. [Auteur]
Pereon, Y. [Auteur]
Salort-Campana, E. [Auteur]
Nadaj-Pakleza, A. [Auteur]
Masingue, M. [Auteur]
Malfatti, Edoardo [Auteur]
Hôpital Henri Mondor
Stojkovic, T. [Auteur]
Villar-Quiles, R. N. [Auteur]

Titre de la revue :

Journal of Neurology, Neurosurgery and Psychiatry

Nom court de la revue :

J Neurol Neurosurg Psychiatry

Numéro :

0

Pagination :

1-9

Éditeur :

BMJ Journals

Date de publication :

2024-11-19

ISSN :

1468-330X

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

Background Myosin heavy chain 7 (MYH7)-related myopathies (MYH7-RMs) are a group of muscle disorders linked to pathogenic variants in the MYH7 gene, encoding the slow/beta-cardiac myosin heavy chain, which is highly expressed ...
Lire la suite >Background Myosin heavy chain 7 (MYH7)-related myopathies (MYH7-RMs) are a group of muscle disorders linked to pathogenic variants in the MYH7 gene, encoding the slow/beta-cardiac myosin heavy chain, which is highly expressed in skeletal muscle and heart. The phenotype is heterogeneous including distal, predominantly axial or scapuloperoneal myopathies with variable cardiac involvement. Methods We retrospectively analysed the clinical, muscle MRI, genetic and myopathological features of 57 MYH7 patients. Patients received a thorough neurological (n=57, 100%), cardiac (n=51, 89%) and respiratory (n=45, 79%) assessment. Muscle imaging findings and muscle biopsies were reappraised in 19 (33%) and 27 (47%) patients, respectively. Results We identified three phenotypes with varying degrees of overlap: distal myopathy (70%), scapuloperoneal (23%) and axial with peculiar cervical spine rigidity called the ‘sphinx’ phenotype (7%). 14% of patients had either dilated cardiomyopathy, hypertrophic cardiomyopathy or left ventricular non-compaction cardiomyopathy. 31% of patients had prominent respiratory involvement, including all patients with the ‘sphinx’ phenotype. Muscle MRI showed involvement of tibialis anterior, followed by quadriceps, and erector spinae in patients with axial phenotype. Cores represented the most common myopathological lesion. We report 26 pathogenic variants of MYH7 gene, 9 of which are novel. Conclusions MYH7-RMs have a large phenotypic spectrum, including distal, scapuloperoneal or axial weakness, and variable cardiac and respiratory involvement. Tibialis anterior is constantly and precociously affected both clinically and on muscle imaging. Cores represent the most common myopathological lesion. Our detailed description of MYH7-RMs should improve their recognition and management.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

Université de Lille
Inserm
CHU Lille

Collections :

• Lille Neurosciences & Cognition (LilNCog) - U 1172

Date de dépôt :

2024-11-22T22:05:44Z
2024-12-04T08:33:21Z