Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein we discuss the details of a patient\u27s case of adult onset CNM. We also highlight the unique features of this case with regards to the importance of electromyography (EMG), muscle biopsy and genetic testing in identifying CNM, as well as potential for improving outcomes by having a high index or suspicion and emphasizing better access to healthcare in underserved areas
Centronuclear myopathy (CNM) is a genetically heterogeneous disorder associated with general skeleta...
Abstract Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinic...
International audienceCentronuclear myopathy (CNM) is a genetically heterogeneous disorder associate...
Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein ...
Centronuclear myopathy (CNM) is a group of rare genetic muscle disorders characterized by muscle fib...
Centronuclear myopathy (CNM) is a genetically heterogeneous disorder associated with general skeleta...
Centronuclear myopathy (CNM) is a slowly progressive congenital myopathy characterized by abnormal c...
BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuc...
Dynamin2 (DNM2) gene mutations may result in Charcot-Marie-Tooth disease and centronuclear myopathy....
Centronuclear myopathy (CNM) is a genetically heterogeneous congenital myopathy characterized by mus...
Centronuclear myopathy (CNM) is a genetically heterogeneous disorder associated with general skeleta...
Abstract Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinic...
International audienceCentronuclear myopathy (CNM) is a genetically heterogeneous disorder associate...
Dynamin 2 (DMN2) mutations cause centronuclear myopathy (CNM) and Charcot Marie Tooth (CMT). Herein ...
Centronuclear myopathy (CNM) is a group of rare genetic muscle disorders characterized by muscle fib...
Centronuclear myopathy (CNM) is a genetically heterogeneous disorder associated with general skeleta...
Centronuclear myopathy (CNM) is a slowly progressive congenital myopathy characterized by abnormal c...
BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuc...
Dynamin2 (DNM2) gene mutations may result in Charcot-Marie-Tooth disease and centronuclear myopathy....
Centronuclear myopathy (CNM) is a genetically heterogeneous congenital myopathy characterized by mus...
Centronuclear myopathy (CNM) is a genetically heterogeneous disorder associated with general skeleta...
Abstract Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinic...
International audienceCentronuclear myopathy (CNM) is a genetically heterogeneous disorder associate...