Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosis

BACKGROUND AND OBJECTIVE: TK2 deficiency (TK2d) is a rare mitochondrial disorder that manifests predominantly as a progressive myopathy with a broad spectrum of severity and age of onset. The rate of progression is variable, and the prognosis is poor due to early and severe respiratory involvement....

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Detalles Bibliográficos
Autores principales: Domínguez-González, Cristina, Fernández-Torrón, Roberto, Moore, Ursula, de Fuenmayor-Fernández de la Hoz, Carlos Pablo, Vélez-Gómez, Beatriz, Cabezas, Juan Antonio, Alonso-Pérez, Jorge, González-Mera, Laura, Olivé, Montse, García-García, Jorge, Moris, Germán, León Hernández, Juan Carlos, Muelas, Nuria, Servian-Morilla, Emilia, Martin, Miguel A., Díaz-Manera, Jordi, Paradas, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217784/
https://www.ncbi.nlm.nih.gov/pubmed/35286480
http://dx.doi.org/10.1007/s00415-021-10957-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217784/
https://www.ncbi.nlm.nih.gov/pubmed/35286480
http://dx.doi.org/10.1007/s00415-021-10957-0

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