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一种罕见的夏科-马里-图思(Charcot-Marie-Tooth)表型,与髓鞘蛋白零(myelin protein zero)细胞内域的突变有关。

Unusual Charcot-Marie-Tooth phenotype due to a mutation within the intracellular domain of myelin protein zero.

机构信息

Department of Neurology, St. Josef-Hospital, Ruhr-University Bochum, Gudrunstrasse 56, 44791 Bochum, Germany.

出版信息

Muscle Nerve. 2010 Apr;41(4):550-4. doi: 10.1002/mus.21523.

Abstract

Myelin protein zero (MPZ/P0) constitutes a major component of compact peripheral myelin. We report a family with a missense mutation, c.700G>T p.Asp234Tyr (deviant nomenclature: c.670G>T, p.Asp224Tyr), within the intracellular domain of myelin protein zero, who has distal sensorimotor symptoms, cramps, restless legs syndrome, neuropathic pain, and carpal tunnel syndrome. The index patient responded to intravenous immunoglobulin and immunosuppression, so there may be a possible secondary autoimmune process, probably triggered by altered antigen presentation due to mutated MPZ protein.

摘要

髓鞘蛋白零 (MPZ/P0) 构成致密周围髓鞘的主要成分。我们报告了一个家族,其在髓鞘蛋白零的细胞内域中存在错义突变 c.700G>T p.Asp234Tyr(异常命名法:c.670G>T,p.Asp224Tyr),该家族患者具有远端感觉运动症状、痉挛、不宁腿综合征、神经病理性疼痛和腕管综合征。索引患者对静脉注射免疫球蛋白和免疫抑制有反应,因此可能存在潜在的自身免疫过程,可能是由于突变的 MPZ 蛋白导致抗原呈递改变而触发的。

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