新描述的末端截断LAMB1变异的临床放射谱的扩展。

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
Hélène Morel, Laurent Bailly, Cédric Urbanczyk, Dominique Hervé, Stéphane Berroir, Raphaël Le Bouc, Richard Levy, Mylène Meyer, Chaker Aloui, Elisabeth Tournier-Lasserve, Guillaume Mathey
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引用次数: 0

摘要

目的:完善最近发现的与LAMB1末端截断致病变异相关的表型的临床谱。方法:对2个不相关家族6例分离末端截断型LAMB1变异的患者进行详细的临床、神经心理学和MRI调查。结果:所有患者均存在LAMB1末端截断致病性变异。在所有4例年龄大于50岁的患者中均观察到海马型情景记忆功能障碍与弥漫性脑白质病的特异性关联,其中2例患者在数年随访中随着时间的推移略有恶化。其他非特异性神经系统症状也有报道,如这4例患者和2例年轻患者出现麻木、语言障碍或晕厥。讨论:广泛脑白质病与海马型情景记忆功能障碍的关联强烈提示50岁以上成人LAMB1末端截断变异。早期认知疾病和影像异常可能在几十年前就存在了。可以观察到其他短暂的表现,这种关联应该导致LAMB1筛查,以避免不必要的侵入性调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating <i>LAMB1</i> Variations.

Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating <i>LAMB1</i> Variations.

Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating <i>LAMB1</i> Variations.

Extension of the Clinicoradiologic Spectrum of Newly Described End-Truncating LAMB1 Variations.

Objectives: To refine the clinical spectrum of a very recently identified phenotype associated with LAMB1 end-truncating pathogenic variations.

Methods: Detailed clinical, neuropsychological, and MRI investigation of 6 patients from 2 unrelated families segregating end-truncating LAMB1 variations.

Results: All patients harbored a LAMB1 end-truncating pathogenic variation. The specific association of a hippocampal type episodic memory dysfunction and a diffuse leukoencephalopathy was observed in all 4 patients aged older than 50 years, slightly worsening over time in 2 patients with several years of follow-up. Additional unspecific neurologic symptoms are reported, such as episodes of numbness, language troubles, or faintness in these 4 patients and the 2 younger ones.

Discussion: The association of an extensive leukoencephalopathy with an episodic memory dysfunction of the hippocampal type is strongly suggestive of a LAMB1 end-truncating variation in adults older than 50 years. Early cognitive complaints and imaging abnormalities might exist decades before. Additional transient manifestations can be observed, and this association should lead to LAMB1 screening to avoid unnecessary invasive investigations.

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来源期刊
Neurology-Genetics
Neurology-Genetics Medicine-Neurology (clinical)
CiteScore
6.30
自引率
3.20%
发文量
107
审稿时长
15 weeks
期刊介绍: Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. Original articles in all areas of neurogenetics will be published including rare and common genetic variation, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease-genes, and genetic variations with a putative link to diseases. This will include studies reporting on genetic disease risk and pharmacogenomics. In addition, Neurology: Genetics will publish results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials are welcome, including well-powered studies reporting negative results.
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