Homozygous SOD1 Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian Family. (February 2022)

• Record Type: Journal Article
• Authors: Gagliardi, Delia; Ahmadinejad, Minoo; Del Bo, Roberto; Meneri, Megi; Comi, Giacomo Pietro; Corti, Stefania; Ronchi, Dario
• Is Part Of: Neurology. Volume 8:Number 1(2022)
• Publication Date: 2022-02
• Subjects: Neurogenetics -- Periodicals; 616.80442
• DOI: 10.1212/NXG.0000000000000645
• Languages: English
• ISSNs: 2376-7839

Abstract

Abstract : Objectives: Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder characterized by degeneration of motor neurons determining progressive muscular atrophy, weakness, and death from respiratory failure. Methods: Here, we report clinical and molecular findings of a novel Iranian family affected with a severe form of early-onset familial ALS. Results: Three siblings born to consanguineous parents developed a form of ALS characterized by early-onset lower limb involvement and a fast progression, proving fatal at age 16 years for 1 of them. Molecular analysis of the SOD1 gene revealed the homozygous substitution c.434T>C in exon 5 resulting in the amino acid change p.Leu144Ser (L144S), previously reported as a dominant variant. Both parents were heterozygous carriers. The probands' mother recently developed a late-onset ALS with predominant upper motor neuron involvement. Discussion: This report adds p.L144S to the short list of homozygous SOD1 variants and suggests that the development of an earlier-onset and/or faster disease progression can occur when 2 mutated alleles are present.