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

IF 1.6 4区 医学 Q3 CLINICAL NEUROLOGY Neurogenetics Pub Date : 2024-04-01 Epub Date: 2024-02-09 DOI:10.1007/s10048-024-00749-9
Ettore Cioffi, Gianluca Coppola, Olimpia Musumeci, Salvatore Gallone, Gabriella Silvestri, Salvatore Rossi, Fiorella Piemonte, Jessica D'Amico, Alessandra Tessa, Filippo Maria Santorelli, Carlo Casali
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引用次数: 0

摘要

遗传性痉挛性截瘫(HSP)是一组主要影响脊柱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、早发的常染色体隐性遗传 HSP,与 GBA2 双重复突变有关。全世界已描述了约 30 个家族,这些家族具有不同的表型,如复杂 HSP、隐性小脑共济失调或马内斯科-斯约格伦综合征(Marinesco-Sjögren Syndrome)。在此,我们报告了五名携带五种新型 GBA2 突变的 SPG46 患者,这是迄今为止在意大利描述的最大系列。患者在五个不同的中心接受了神经系统检查、临床认知评估、脊柱侧弯评估的柱状成像、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,具有上凝视麻痹和运动障碍等显著特征。我们回顾了现有文献中所有病例的人口统计学、遗传学、生物化学和临床信息,重点关注病例的全球分布、该综合征的特征、多变的表现形式、新的潜在识别特征以及测量 GBA2 酶活性的意义。
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Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature.

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.

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来源期刊
Neurogenetics
Neurogenetics 医学-临床神经学
CiteScore
3.90
自引率
0.00%
发文量
24
审稿时长
6 months
期刊介绍: Neurogenetics publishes findings that contribute to a better understanding of the genetic basis of normal and abnormal function of the nervous system. Neurogenetic disorders are the main focus of the journal. Neurogenetics therefore includes findings in humans and other organisms that help understand neurological disease mechanisms and publishes papers from many different fields such as biophysics, cell biology, human genetics, neuroanatomy, neurochemistry, neurology, neuropathology, neurosurgery and psychiatry. All papers submitted to Neurogenetics should be of sufficient immediate importance to justify urgent publication. They should present new scientific results. Data merely confirming previously published findings are not acceptable.
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