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遗传性痉挛性截瘫 46 型(SPG46):意大利大型病例系列中的新 GBA2 变异体及文献复习。

Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature.

机构信息

Department of Medico-Surgical Sciences and Biotechnologies, University of Rome Sapienza, Latina, Italy.

Department of Experimental and Clinical Medicine, University of Messina, Messina, Italy.

出版信息

Neurogenetics. 2024 Apr;25(2):51-67. doi: 10.1007/s10048-024-00749-9. Epub 2024 Feb 9.

DOI:10.1007/s10048-024-00749-9
PMID:38334933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11076336/
Abstract

Hereditary spastic paraparesis (HSP) is a group of central nervous system diseases primarily affecting the spinal upper motor neurons, with different inheritance patterns and phenotypes. SPG46 is a rare, early-onset and autosomal recessive HSP, linked to biallelic GBA2 mutations. About thirty families have been described worldwide, with different phenotypes like complicated HSP, recessive cerebellar ataxia or Marinesco-Sjögren Syndrome. Herein, we report five SPG46 patients harbouring five novel GBA2 mutations, the largest series described in Italy so far. Probands were enrolled in five different centres and underwent neurological examination, clinical cognitive assessment, column imaging for scoliosis assessment, ophthalmologic examination, brain imaging, GBA2 activity in peripheral blood cells and genetic testing. Their phenotype was consistent with HSP, with notable features like upper gaze palsy and movement disorders. We review demographic, genetic, biochemical and clinical information from all documented cases in the existing literature, focusing on the global distribution of cases, the features of the syndrome, its variable presentation, new potential identifying features and the significance of measuring GBA2 enzyme activity.

摘要

遗传性痉挛性截瘫(HSP)是一组主要影响脊髓上运动神经元的中枢神经系统疾病,具有不同的遗传模式和表型。SPG46 是一种罕见的早发性常染色体隐性 HSP,与双等位基因 GBA2 突变有关。全世界约有三十个家族被描述,具有不同的表型,如复杂 HSP、隐性小脑共济失调或 Marinesco-Sjögren 综合征。在此,我们报告了五例 SPG46 患者,他们携带五种新的 GBA2 突变,这是迄今为止在意大利描述的最大系列。先证者在五个不同的中心被招募,并接受了神经系统检查、临床认知评估、脊柱侧弯评估的柱成像、眼科检查、脑成像、外周血细胞中的 GBA2 活性和基因检测。他们的表型与 HSP 一致,具有明显的特征,如上凝视麻痹和运动障碍。我们回顾了所有已发表文献中记录的病例的人口统计学、遗传学、生化和临床信息,重点关注病例的全球分布、综合征的特征、其可变表现、新的潜在识别特征以及测量 GBA2 酶活性的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b7c/11076336/62cb586929f6/10048_2024_749_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b7c/11076336/74ffe54e89ff/10048_2024_749_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b7c/11076336/62cb586929f6/10048_2024_749_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b7c/11076336/74ffe54e89ff/10048_2024_749_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b7c/11076336/62cb586929f6/10048_2024_749_Fig2_HTML.jpg

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本文引用的文献

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Neurologia (Engl Ed). 2023 Jun;38(5):372-374. doi: 10.1016/j.nrleng.2022.06.009. Epub 2023 Apr 7.
2
The Role of Primary Mitochondrial Disorders in Hearing Impairment: An Overview.原发性线粒体疾病在听力障碍中的作用:概述。
Medicina (Kaunas). 2023 Mar 19;59(3):608. doi: 10.3390/medicina59030608.
3
Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement.
一个伴有小脑受累的痉挛性截瘫台湾队列的临床和遗传学特征
Front Neurol. 2022 Sep 30;13:1005670. doi: 10.3389/fneur.2022.1005670. eCollection 2022.
4
Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts.不完全显性与可变表达:从临床研究到人群队列
Front Genet. 2022 Jul 25;13:920390. doi: 10.3389/fgene.2022.920390. eCollection 2022.
5
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype.痉挛性截瘫 46 型:痉挛性共济失调表型的意大利复合杂合子患者中新型和复发性 GBA2 基因突变。
Neurol Sci. 2021 Nov;42(11):4741-4745. doi: 10.1007/s10072-021-05463-0. Epub 2021 Jul 12.
6
Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in gene in a large consanguineous Saudi family.沙特一个大家族中因一个基因的罕见突变导致的伴有痉挛的常染色体隐性小脑共济失调。
Genes Dis. 2019 Jul 27;8(1):110-114. doi: 10.1016/j.gendis.2019.07.009. eCollection 2021 Jan.
7
SPG46 due to truncating mutations in GBA2: Two cases from India.因GBA2基因截短突变导致的SPG46:来自印度的两例病例。
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