Department of Medico-Surgical Sciences and Biotechnologies, University of Rome Sapienza, Latina, Italy.
Department of Experimental and Clinical Medicine, University of Messina, Messina, Italy.
Neurogenetics. 2024 Apr;25(2):51-67. doi: 10.1007/s10048-024-00749-9. Epub 2024 Feb 9.
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.
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。