A novel missense COL9A3 variant in a pedigree with multiple lumbar disc herniation.

J Orthop Surg Res

Department of Orthopedics, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, N1# Shangcheng Road, Yiwu, 322000, Zhejiang Province, China.

Published: January 2024

AI Article Synopsis

  • - A novel pathogenic variant in the COL9A3 gene was discovered in a family with a history of lumbar disc herniation (LDH), particularly affecting a 14-year-old boy and multiple relatives diagnosed at young ages.
  • - Whole exome sequencing identified a heterozygous missense variant (c.1150C > T, p.Arg384Trp) in the COL9A3 gene, which is considered pathogenic based on ACMG guidelines.
  • - Computational predictions suggest that this variant makes the COL9A3 protein less stable and alters its charge properties and spatial conformation, enhancing the understanding of how mutations in this gene contribute to LDH.

Article Abstract

Trp3 allele in COL9A3 gene has been widely studied in populations with intervertebral disc disease. We identified a novel pathogenic variant in COL9A3 gene in a pedigree with multiple lumbar disc herniation (LDH). The proband was a 14-year-old boy who developed LDH at the L4/5 and L5/S1 spinal segments. His father, paternal aunt and grandfather were diagnosed with LDH at an age of 35, 30 and 23, respectively. By applying whole exome sequencing, a heterozygous missense variant (c.1150C > T, p.Arg384Trp) in COL9A3 was identified. According to the ACMG guidelines, this variant is predicted to be pathogenic. In addition, prediction tools found COL9A3 protein of this variant a reduced stability, some changed charge properties, and an altered spatial conformation. Findings expanded the mutational spectrum of LDH and contributed to the understanding of COL9A3 in the pathogenesis of LDH.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10762954PMC
http://dx.doi.org/10.1186/s13018-023-04481-2DOI Listing

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