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与IgM单克隆丙种球蛋白病相关的神经病变中的细胞遗传学异常。

Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy.

作者信息

Eurelings Marijke, Lokhorst Henk M, Notermans Nicolette C, Krijtenburg Pieter Jaap, Kessel Berris van, Eleveld Mark J, Bloem Andries, Wokke John H, Poot Martin, Buijs Arjan

机构信息

Department of Neurology, the Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, The Netherlands.

出版信息

J Neurol Sci. 2007 Sep 15;260(1-2):124-31. doi: 10.1016/j.jns.2007.04.022. Epub 2007 Jun 1.

Abstract

The occurrence and nature of cytogenetic aberrations in polyneuropathy associated with IgM monoclonal gammopathy was determined. Therefore, interphase fluorescence in situ hybridization (FISH) was applied in 22 patients with polyneuropathy associated with IgM monoclonal gammopathy, multiplex ligation-dependent probe amplification (MLPA) assay in 18 of these patients and genome-wide-array-based comparative genomic hybridization (CGH) in eight of these 18 patients. Four patients had 10-20% and one patient had 30% B cells with IgH rearrangements; one patient had additional loss of 14qter; one patient had amplification of 6p and loss of 6q. Cytogenetic aberrations may be found in one third of the patients with neuropathy associated with IgM monoclonal gammopathy and are mainly associated with indolent Waldenstrom's Macroglobulinemia.

摘要

确定了与IgM单克隆丙种球蛋白病相关的多神经病中细胞遗传学异常的发生情况及性质。因此,对22例与IgM单克隆丙种球蛋白病相关的多神经病患者进行了间期荧光原位杂交(FISH)检测,对其中18例患者进行了多重连接依赖探针扩增(MLPA)分析,对这18例患者中的8例进行了基于全基因组阵列的比较基因组杂交(CGH)检测。4例患者有10%-20%的B细胞发生IgH重排,1例患者有30%的B细胞发生IgH重排;1例患者有14qter额外缺失;1例患者有6p扩增和6q缺失。细胞遗传学异常可能在三分之一的与IgM单克隆丙种球蛋白病相关的神经病患者中发现,且主要与惰性华氏巨球蛋白血症相关。

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