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Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations

BACKGROUND: Lipid storage myopathy (LSM) is a genetically heterogeneous group with variable clinical phenotypes. Late-onset multiple acyl-coenzyme A dehydrogenation deficiency (MADD) is a rather common form of LSM in China. Diagnosis and clinical management of it remain challenging, especially witho...

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Detalles Bibliográficos
Autores principales: Liu, Xin-Yi, Jin, Ming, Wang, Zhi-Qiang, Wang, Dan-Ni, He, Jun-Jie, Lin, Min-Ting, Fu, Hong-Xia, Wang, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910365/
https://www.ncbi.nlm.nih.gov/pubmed/27270537
http://dx.doi.org/10.4103/0366-6999.183423