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An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member
Authors:Francesca Trojsi  Giovanni Piccirillo  Cinzia Femiano  Raffaele Damiano  Maria Rosaria Monsurrò
Affiliation:1. Department of Medical, Surgical, Neurological, Metabolic and Aging Sciences, Second University of Naples, 80138 Naples, Italy;;2. Magnetic Resonance Imaging Center SUN-FISM, Neurological Institute for Diagnosis and Care Hermitage Capodimonte, Naples, Italy
Abstract:
We report the first Italian kindred with Familial Amyotrophic Lateral Sclerosis (FALS) due to c.149T>C mutation in the exon 5 of superoxide dismutase-1 (SOD1) gene. The proband was a 49-year-old woman who came to our observation because of an history of progressive limbs weakness and gait impairment. She belonged to a family of 24 affected members. The prevalent phenotype of the affected members was characterized by slowly progressive spinal impairment with proximal distribution of weakness, and bulbar involvement in advanced stages. We briefly reviewed the few previous reports about the same SOD1 mutation and discussed the hypothesis that structural instability of the mutant codon 149 protein may underlie some toxic effects significantly involved in FALS pathogenesis.Key words: Familial ALS (FALS), superoxide dismutase 1 (SOD1), mutation
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