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Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations

2021; Elsevier BV; Volume: 429; Linguagem: Inglês

10.1016/j.jns.2021.118062

1878-5883

Raquel Baviera‐Muñoz, Marina Campins‐Romeu, Lidón Carretero‐Vilarroig, Isabel Sastre‐Bataller, Irene Martínez‐Torres, Juan F. Vázquez‐Costa, Nuria Muelas, Teresa Sevilla, Juan J. Vílchez, Elena Aller, Teresa Jaijo, Luís Bataller, Carmen Espinós,

Genetic Neurodegenerative Diseases

Spastic paraplegia type 7 (SPG7) is one of the most common hereditary spastic paraplegias. SPG7 mutations most often lead to spastic paraparesis (HSP) and/or hereditary cerebellar ataxia (HCA), frequently with mixed phenotypes. We sought to clinically and genetically characterize a Spanish cohort of SPG7 patients. Patients were recruited from our HCA and HSP cohorts. We identified twenty-one patients with biallelic pathogenic SPG7 mutations. Mean age at onset was 37.4 years (SD ± 14.3). The most frequent phenotype was spastic ataxia (57%), followed by pure spastic paraplegia (19%) and complex phenotypes (19%). Isolated patients presented with focal or multifocal dystonia, subclinical myopathy or ophthalmoplegia. p.Ala510Val was the most frequent pathogenic variant encountered. Compound heterozygous for p.Ala510Val displayed younger onset (p < 0.05) and more complex phenotypes (p < 0.05) than p.Ala510Val homozygotes. Two novel variants were found: p.Lys559Argfs*33 and p.Ala312Glu. In conclusion, spastic ataxia is the most common phenotype found in Spanish patients. Nonetheless, SPG7 analysis should also be considered in patients with less frequent clinical findings such as dystonia or ophthalmoplegia especially when these symptoms are associated with mild spastic ataxia.