Journal of Multiple Sclerosis
ISSN - 2376-0389NLM - 101654564
Jenny E Hinshaw
Tanzania
Review Article
Progressive Neuromuscular Syndromes Linked to Dynamin-2 Mutations
Author(s): Neil M Renwick, Lev G Goldfarb, Nyamkhishig Sambuughin, Jenny E Hinshaw, Camilo Toro and Yodor A PlatonovNeil M Renwick, Lev G Goldfarb, Nyamkhishig Sambuughin, Jenny E Hinshaw, Camilo Toro and Yodor A Platonov
Mutations in dynamin-2 are associated with several neuromuscular disorders, including two forms of Charcot- Marie-Tooth disease, axonal CMT2M and intermediate CMTDIB, Centronuclear myopathy ADCNM, Lethal congenital contractures syndrome type 5 LCCS5, and Hereditary spastic paraplegia SPG. Each disorder manifests with muscle weakness and atrophy, however the cause of weakness is due to damage to peripheral nerves in CMT2M and CMTDIB, skeletal muscle degeneration in ADCNM, and disturbances in the upper motor neurons and/or corticospinal tracts in SPG. Pathogenic effects of mutations may result from domain-specific structural and functional disruptions. ADCNMcausing mutations cluster at the interface between the Stalk and Pleckstrin homology domains, whereas CMT-related mutations occur in the part of the Pleckstrin homology domain adjoining the C-terminal Proline/arginine-rich domain. Th.. View More»
