Recessive distal motor neuropathy with pyramidal signs in an Omani kindred: underlying novel mutation in the SIGMAR1 gene. (12th December 2017)

• Record Type: Journal Article
• Authors: Nandhagopal, R.; Meftah, D.; Al‐Kalbani, S.; Scott, P.
• Is Part Of: European journal of neurology. Volume 25:Number 2(2018)
• Page Start: 395
• Page End: 403
• Publication Date: 2017-12-12
• Subjects: autosomal recessive inheritance -- distal hereditary motor neuropathy -- Omani kindred -- SIGMAR1 mutation; Neurology -- Periodicals; Nervous system -- Diseases -- Periodicals; 616.8
• DOI: 10.1111/ene.13519
• Languages: English
• ISSNs: 1351-5101

Abstract

Abstract : Background and purpose: Distal hereditary motor neuropathy (dHMN) due to sigma non‐opioid intracellular receptor 1 ( SIGMAR1 ) gene mutation (OMIM 601978.0003) is a rare neuromuscular disorder characterized by prominent amyotrophic distal limb weakness and co‐existing pyramidal signs initially described in a Chinese family recently. We report an extended consanguineous Omani family segregating dHMN with pyramidal signs in an autosomal recessive pattern and describe a novel mutation in the SIGMAR1 gene underlying this motor phenotype. We also provide an update on the reported phenotypic profile of SIGMAR1 mutations. Methods: We utilized homozygosity mapping and whole‐exome sequencing of leucocyte DNA obtained from three affected members of an Omani family who manifested with a length‐dependent motor neuropathy and pyramidal signs. Results: We identified a novel C>T transition at nucleotide position 238 (c.238C>T) in exon 2 of the SIGMAR1 gene. Sanger sequencing and segregation analysis confirmed the presence of two copies of the variant in the affected subjects, unlike the unaffected healthy parents/sibling who carried, at most, a single copy. The T allele is predicted to cause a truncating mutation (p.Gln80*), probably flagging the mRNA for nonsense‐mediated decay leading to a complete loss of function, thereby potentially contributing to the disease process. Conclusions: Our finding expands the spectrum of SIGMAR1 mutations causing recessive dHMN and indicates that this disorder is pan‐ethnic. SIGMAR1 mutation should be included in the diagnostic panel of a dHMN, especially if there are co‐existing pyramidal signs and autosomal recessive inheritance.