Unraveling SPG46 : Clinical, Genetic, and Neuroimaging Features
Year: 2026
Type: article
Abstract: BACKGROUND: SPG46 is an autosomal recessive hereditary spastic paraplegia (HSP) caused by biallelic GBA2 mutations. As a rare and still poorly understood condition, information about its clinical and genetic spectrum is scarce. OBJECTIVE: This study aimed to delineate the clinical, neuroimaging, and genetic characteristics of a Brazilian SPG46 cohort. METHODS: We conducted a retrospective cross-sectional study at two referral centers, identifying nine patients from six unrelated families harboring pathogenic GBA2 variants through whole-exome sequencing. Demographic, clinical, neuroimaging, and genetic data were systematically analyzed. RESULTS: The cohort (4 males, 5 females) presented disease onset between 6 and 24 years (mean, 10.7). All exhibited progressive spastic paraplegia associated with cerebellar ataxia, dysarthria, and cognitive impairment. Psychiatric manifestations, sleep disturbances, skeletal deformities, and dystonia were frequent. Cerebellar atrophy was observed in four cases, whereas corpus callosum thinning, cataracts, and hearing impairment were absent. CONCLUSION: The recurrent GBA2 c.1365G>C;p.(Trp455Cys) variant suggests a potential founder effect and expands the phenotypic spectrum of SPG46 in Brazil.
DOI: 10.1002/mdc3.70733
Authors: Raphael Pinheiro Camurugy da Hora, Victor Rebelo Procaci, Júlian Letícia Freitas, Fabrício Diniz de Lima, Anna Maria Gomes, Thiago Yoshinaga Tonholo Silva, Pedro Fraiman, Maria Thereza Drumond Gama, Katiane Raisa Servelhere, Marcondes Cavalcante de França Júnior, Orlando Graziani Povoas Barsottini, José Luiz Pedroso
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W7170140060