Yabe I, Higashi T, Kikuchi S, Sasaki H, Fukazawa T, Yoshida K, Tashiro K
Department of Neurology, Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan.
Neurology. 2003 Aug 12;61(3):384-6. doi: 10.1212/01.wnl.0000061520.63546.8f.
The authors describe a family in which two individuals have clinical distal myopathy with rimmed vacuoles (DMRV). While the clinical and most of the pathologic features in these patients were compatible with a diagnosis of DMRV, the presence of inflammatory changes in the connective tissue between muscle fibers was not. Gene analysis revealed a compound heterozygous mutation in these individuals, characterized by V572L and I472T.
作者描述了一个家族,其中两名个体患有伴有镶边空泡的临床远端肌病(DMRV)。虽然这些患者的临床和大多数病理特征与DMRV的诊断相符,但肌纤维之间结缔组织中的炎症变化却不相符。基因分析显示这些个体存在复合杂合突变,其特征为V572L和I472T。