Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes

Jordi Díaz-Manera*, Aida Alejaldre, Laura González, Montse Olivé, David Gómez-Andrés, Nuria Muelas, Juan José Vílchez, Jaume Llauger, Pilar Carbonell, Celedonio Márquez-Infante, Roberto Fernández-Torrón, Juan José Poza, Adolfo López de Munáin, Lidia González-Quereda, Sonia Mirabet, Jordi Clarimon, Pía Gallano, Ricard Rojas-García, Eduard Gallardo, Isabel Illa

*Autor corresponent d’aquest treball

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Resum

© 2015 Elsevier B.V. Identifying the mutated gene that produces a particular muscle dystrophy is difficult because different genotypes may share a phenotype and vice versa. Muscle MRI is a useful tool to recognize patterns of muscle involvement in patients with muscle dystrophies and to guide the diagnosis process. The radiologic pattern of muscle involvement in patients with mutations in the EMD and LMNA genes has not been completely established. Our objective is to describe the pattern of muscle fatty infiltration in patients with mutations in the EMD and in the LMNA genes and to search for differences between the two genotypes that could be helpful to guide the genetic tests. We conducted a national multicenter study in 42 patients, 10 with mutations in the EMD gene and 32 with mutations in the LMNA gene. MRI or CT was used to study the muscles from trunk to legs. Patients had a similar pattern of fatty infiltration regardless of whether they had the mutation in the EMD or LMNA gene. The main muscles involved were the paravertebral, glutei, quadriceps, biceps, semitendinosus, semimembranosus, adductor major, soleus, and gastrocnemius. Involvement of peroneus muscle, which was more frequently affected in patients with mutations in the EMD gene, was useful to differentiate between the two genotypes. Muscle MRI/CT identifies a similar pattern of muscle fatty infiltration in patients with mutations in the EMD or the LMNA genes. The involvement of peroneus muscles could be useful to conduct genetic analysis in patients with an EDMD phenotype.
Idioma originalEnglish
Pàgines (de-a)33-40
RevistaNeuromuscular Disorders
Volum26
Número1
DOIs
Estat de la publicacióPublicada - 1 de gen. 2016

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