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一名患有摇臀症突变、X连锁痉挛性截瘫/佩利措伊斯-梅茨巴赫病和赖氨酸尿症的男童。

A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.

作者信息

Naidu S, Dlouhy S R, Geraghty M T, Hodes M E

机构信息

Kennedy Krieger Institute, Baltimore, Maryland, USA.

出版信息

J Inherit Metab Dis. 1997 Nov;20(6):811-6. doi: 10.1023/a:1005328019832.

Abstract

A 3.5-year-old boy had intact cognition, delayed walking, progressive spastic paraparesis and congenital nystagmus. The mother denied family history of any neurological disorders, so an extensive work-up was begun. Lysinuria, increased signal on cerebral T2-weighted MRI imaging and the rumpshaker mutation (Ile186Thr) in his proteolipid protein gene. PLP, were found. When faced with these facts, the mother admitted that she was related to the family reported by Johnston and McKusick in 1962 and Kobayashi in 1994, in whom this mutation has been reported. This is the first report of an abnormal MRI scan in this family.

摘要

一名3.5岁男童认知功能正常,但行走延迟、进行性痉挛性截瘫且患有先天性眼球震颤。其母亲否认家族中有任何神经疾病史,因此展开了全面检查。结果发现患儿存在赖氨酸尿症、脑部T2加权磁共振成像(MRI)信号增强以及其蛋白脂蛋白基因(PLP)中的摇臀者突变(Ile186Thr)。面对这些事实,患儿母亲承认自己与1962年约翰斯顿和麦库西克以及1994年小林所报道的家族有亲缘关系,在该家族中曾报道过这种突变。这是该家族中首次出现MRI扫描异常的报告。

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