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Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variants.
Ma, Maxwell T; Chen, Dong-Hui; Raskind, Wendy H; Bird, Thomas D.
Afiliação
  • Ma MT; Department of Neurology, University of Washington, 1660 S. Columbian way S127, Seattle WA, United States; Department of Neurology, VA Puget Sound Medical Center, United States. Electronic address: Mamax@UW.edu.
  • Chen DH; Department of Neurology, University of Washington, 1660 S. Columbian way S127, Seattle WA, United States.
  • Raskind WH; Department of Medicine, University of Washington, United States; Department of Psychiatry and Behavioral Sciences, United States; GRECC, VA Medical Center, United States; MIRECC, VA Medical Center, United States.
  • Bird TD; Department of Neurology, University of Washington, 1660 S. Columbian way S127, Seattle WA, United States; Department of Medicine, University of Washington, United States; Department of Psychiatry and Behavioral Sciences, United States; GRECC, VA Medical Center, United States.
Neuromuscul Disord ; 30(7): 572-575, 2020 07.
Article em En | MEDLINE | ID: mdl-32600828
Distal hereditary motor neuropathy (dHMN) is an inherited neuromuscular disease characterized by symmetric distal weakness and atrophy without sensory changes. There are about thirty known genes associated with dHMN, but together they explain only about a third of cases. Mutations in the sigma non-opioid intracellular receptor 1 gene (SIGMAR1) has been linked to autosomal recessive dHMN with pyramidal signs in several families. This phenotype can mimic amyotrophic lateral sclerosis (ALS). We report a 39-year-old man who was referred to our ALS clinic with distal motor weakness and hyperreflexia. Whole exome sequencing identified two novel variants in the SIGMAR1 gene in the proband. Targeted Sanger sequencing of asymptomatic family members confirmed that each carried one of these two variants. Our findings expand the number of known SIGMAR1 pathogenic variants associated with dHMN, which should be clinically distinguished from ALS.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Receptores sigma / Esclerose Lateral Amiotrófica / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Neuromuscul Disord Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Receptores sigma / Esclerose Lateral Amiotrófica / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: Neuromuscul Disord Ano de publicação: 2020 Tipo de documento: Article