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利用下一代测序技术在一个家族中发现的模拟多发性硬化症的SPG2 。

SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing.

作者信息

Rubegni Anna, Battisti Carla, Tessa Alessandra, Cerase Alfonso, Doccini Stefano, Malandrini Alessandro, Santorelli Filippo M, Federico Antonio

机构信息

Molecular Medicine, IRCCS Stella Maris, Pisa, Italy.

Unit of Neurology and Neurometabolic Disorders, Department of Medicine, Surgery and Neurosciences, University of Siena, Italy, Azienda Ospedaliera Universitaria Senese, Siena.

出版信息

J Neurol Sci. 2017 Apr 15;375:198-202. doi: 10.1016/j.jns.2017.01.069. Epub 2017 Jan 27.

DOI:10.1016/j.jns.2017.01.069
PMID:28320130
Abstract

Several single gene disorders can potentially be overlooked in the differential diagnostic evaluation of patients with multiple sclerosis (MS). Pelizaeus-Merzbacher disease and spastic paraplegia type 2 are allelic X-linked disorders associated with defective myelination of the central nervous system and mutations in PLP1. Neurological symptoms are occasionally observed in female carriers of these mutations. Two women - the proposita (Pt1) and her mother (Pt2) - reported walking difficulties since adolescence and showed progressive cognitive decline. Their neurological examinations revealed spastic gait, pyramidal tract involvement and distal muscle atrophy in the legs. Peripheral neuropathy and diffuse white matter (WM) changes on brain MRI were also observed. Both patients had a preliminary diagnosis of primary progressive MS. Using a targeted method in next generation sequencing, the novel heterozygous c.210T>G/p.Y70* in PLP1 was identified in Pt2. The same mutation was also found in Pt1 but not in five healthy relatives. The mutation showed moderate-to-severe skewed X inactivation in tissues, and Western blotting revealed a significant reduction of PLP1 and DM20 in the sural nerve of Pt2. In conclusion a mother and daughter presented an X-linked dominant disorder with skewed X inactivation. The authors suggest that PLP1 testing might be considered in the evaluation of women with spastic paraparesis, cognitive decline and WM changes.

摘要

在对多发性硬化症(MS)患者进行鉴别诊断评估时,几种单基因疾病可能会被忽视。佩利措伊斯-梅茨巴赫病和2型痉挛性截瘫是等位基因X连锁疾病,与中枢神经系统髓鞘形成缺陷及PLP1基因突变有关。这些突变的女性携带者偶尔会出现神经症状。两名女性——先证者(Pt1)及其母亲(Pt2)——自青少年期起就报告有行走困难,并出现进行性认知衰退。她们的神经学检查显示步态痉挛、锥体束受累以及腿部远端肌肉萎缩。还观察到周围神经病变和脑部MRI上弥漫性白质(WM)改变。两名患者初步诊断为原发性进行性MS。通过下一代测序中的靶向方法,在Pt2中鉴定出PLP1基因新的杂合突变c.210T>G/p.Y70*。在Pt1中也发现了相同的突变,但在五名健康亲属中未发现。该突变在组织中显示出中度至重度的X染色体失活偏斜,蛋白质免疫印迹法显示Pt2腓肠神经中PLP1和DM20显著减少。总之,一对母女表现出一种具有X染色体失活偏斜的X连锁显性疾病。作者建议,在评估患有痉挛性截瘫、认知衰退和WM改变的女性时,可能应考虑进行PLP1检测。

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J Neurol Sci. 2017 Apr 15;375:198-202. doi: 10.1016/j.jns.2017.01.069. Epub 2017 Jan 27.
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