Tachi N, Kozuka N, Ohya K, Chiba S, Sasaki K
School of Health Sciences, Sapporo Medical University, Japan.
J Neurol Sci. 1997 Dec 9;153(1):106-9. doi: 10.1016/s0022-510x(97)00202-5.
Mutation of the myelin protein zero (MPZ) gene is associated with a small number of Charcot-Marie-Tooth (CMT) patients. We present a patient with Lys 130 Arg substitution in the extracellular domain who showed tomacula formation in biopsied sural nerve. CMT patients with mutations Ly 96 Glu, Lys 130 Arg and Ile 135 Leu showed tomaculous neuropathy. Present and previously reported investigations suggest that the pathological phenotypes of peripheral nerve are probably related to the mutations of the MPZ gene.
髓磷脂蛋白零(MPZ)基因突变与少数夏科-马里-图斯(CMT)患者相关。我们报告了一名细胞外结构域存在赖氨酸130精氨酸替代的患者,其活检的腓肠神经显示有腊肠体形成。携带Ly 96 Glu、赖氨酸130精氨酸和异亮氨酸135亮氨酸突变的CMT患者表现为腊肠体性神经病。目前及先前报道的研究表明,周围神经的病理表型可能与MPZ基因突变有关。