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集落刺激因子1受体(CSF1R)基因的一种新突变导致伴有球状体的可变白质脑病。

A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroids.

作者信息

La Piana Roberta, Webber Alina, Guiot Marie-Christine, Del Pilar Cortes Maria, Brais Bernard

机构信息

Laboratory of Neurogenetics of Motion, Montreal Neurological Institute, McGill University, 3801 University Street, Room 622, Montreal, QC, H3A 2B4, Canada,

出版信息

Neurogenetics. 2014 Oct;15(4):289-94. doi: 10.1007/s10048-014-0413-1. Epub 2014 Jul 12.

Abstract

Hereditary diffuse leukoencephalopathy with neuroaxonal spheroids is a neurodegenerative disease associated with mutations in the colony-stimulating factor 1 receptor gene (CSF1R). A 44-year-old woman with a 7-year history of depression presented with neurological signs and a recent cognitive decline. The diagnosis of hereditary diffuse leukoencephalopathy with neuroaxonal spheroids was suspected based on the findings of a predominant frontal leukoencephalopathy and neuroaxonal spheroids on brain biopsy. She shares with her mother a novel CSF1R exon 18 missense mutation (c.2350G > A; p.V784M). The mother has a long-standing bipolar disorder and mild multifocal white matter abnormalities in her 70s. This is the first report of hereditary diffuse leukoencephalopathy with neuroaxonal spheroids due to this novel CSF1R missense mutation. Our report suggests that either marked intrafamilial variability or incomplete penetrance can be associated with CSF1R mutations. The observation of a small bone cyst in our patient supports the hypothesis that hereditary diffuse leukoencephalopathy with neuroaxonal spheroids and polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy may belong to a spectrum of overlapping phenotypes.

摘要

伴有神经轴突球状体的遗传性弥漫性白质脑病是一种与集落刺激因子1受体基因(CSF1R)突变相关的神经退行性疾病。一名有7年抑郁症病史的44岁女性出现神经系统体征及近期认知功能减退。根据脑活检发现以额叶为主的白质脑病及神经轴突球状体,怀疑为伴有神经轴突球状体的遗传性弥漫性白质脑病。她与母亲共有一种新的CSF1R外显子18错义突变(c.2350G>A;p.V784M)。母亲患有长期双相情感障碍,70多岁时存在轻度多灶性白质异常。这是首例因这种新的CSF1R错义突变导致的伴有神经轴突球状体的遗传性弥漫性白质脑病报告。我们的报告提示,CSF1R突变可能与明显的家族内变异性或不完全外显率有关。我们患者中观察到的小骨囊肿支持了以下假说,即伴有神经轴突球状体的遗传性弥漫性白质脑病和伴有硬化性白质脑病的多囊性脂膜性骨发育异常可能属于一系列重叠的表型。

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