A Novel LDB3 Mutation Identified in Patients with Late-Onset Myofibrillar Myopathy

Objective: Inherited myopathies are a diverse group of genetic muscle disorders characterized by muscle weakness and dysfunction resulting from mutations in genes with a wide range of biological functions. This study was performed to elucidate genetic causes in a large family with late-onset myofibrillar myopathy.Methods: Whole-exome sequencing was first applied to the proband, and then subsequent filtering process and in silico analysis was performed to determine causative mutation.Results: This study identified an unreported likely pathogenic mutation, p.Met160Ile, in the LIM domain binding 3 (LDB3) gene. This missense mutation showed complete cosegregation with affected individuals and was located at an evolutionarily well-conserved site. Several in silico analyses, along with simulations of three-dimensional structural changes in the mutant protein, predicted its potential pathogenicity.Conclusion: These findings expand the current understanding of the genetic basis of inherited myopathy and underscore the importance of comprehensive genetic analysis in clinical practice.

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Publication Details

Journal
Journal of Electrodiagnosis and Neuromuscular Diseases
Published
2025-12-31
DOI
https://doi.org/10.18214/jend.2025.00031
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

A Novel LDB3 Mutation Identified in Patients with Late-Onset Myofibrillar Myopathy

Ah Jin Lee, Soo Hyun Nam, Nasrin Tamanna, Ki Wha Chung et al.
Journal of Electrodiagnosis and Neuromuscular Diseases
Cardiomyopathy and Myosin Studies
article

A Novel LDB3 Mutation Identified in Patients with Late-Onset Myofibrillar Myopathy

Ah Jin Lee, Soo Hyun Nam, Nasrin Tamanna, Ki Wha Chung, Byung-Ok Choi
article en

Abstract

Objective: Inherited myopathies are a diverse group of genetic muscle disorders characterized by muscle weakness and dysfunction resulting from mutations in genes with a wide range of biological functions. This study was performed to elucidate genetic causes in a large family with late-onset myofibrillar myopathy.Methods: Whole-exome sequencing was first applied to the proband, and then subsequent filtering process and in silico analysis was performed to determine causative mutation.Results: This study identified an unreported likely pathogenic mutation, p.Met160Ile, in the LIM domain binding 3 (LDB3) gene. This missense mutation showed complete cosegregation with affected individuals and was located at an evolutionarily well-conserved site. Several in silico analyses, along with simulations of three-dimensional structural changes in the mutant protein, predicted its potential pathogenicity.Conclusion: These findings expand the current understanding of the genetic basis of inherited myopathy and underscore the importance of comprehensive genetic analysis in clinical practice.

Journal of Electrodiagnosis and Neuromuscular DiseasesVol. 27(3)
Kongju National University (KR), Samsung Medical Center (KR), Sungkyunkwan University (KR)
National Research Foundation, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 30%
Cardiomyopathy and Myosin Studies
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A Novel LDB3 Mutation Identified in Patients with Late-Onset Myofibrillar Myopathy — Ah Jin Lee, Soo Hyun Nam, et al. · Journal of Electrodiagnosis and Neuromuscular Diseases (2025) | TGRS Research Map | TGRS