Work

Case Report: A novel intronic variant of NIPBL gene detected in a child with cornelia de lange syndrome

Year: 2025

Type: article

Abstract: Background Cornelia de Lange syndrome (CdLS) is a genetically heterogeneous disorder involving multi-system organs, causing physical and mental congenital malformation. Nipped-B-like protein (NIPBL) variants are associated with various CdLS phenotypes. Newborns with typical clinical manifestations (intellectual disability, special appearances, and limb malformation) require a diagnosis. However, diagnosing CdLS is challenging on account of its heterogeneity of genotype and phenotype. Methods In this study, molecular analysis was applied, containing whole exome sequencing (WES), reverse transcriptase PCR (RT-PCR), and minigene splicing assays. Results We identified a novel splice-donor variant (NIPBL c.6343 + 1G>A) by WES. RT-PCR and minigene splicing assays were performed to identify the function of the splice-donor variant on subsequent RNA splicing. The variant caused exon 36 to be skipped. A premature termination codon (PTC) appeared subsequently and a truncated protein with a length of 2088 aa was produced. Conclusion A novel pathogenic variant of CdLS is identified, which affects normal mRNA splicing of the NIPBL gene. These findings enrich the knowledge of CdLS gene variants, which may be responsible for developing this rare disease.

Source: Frontiers in Genetics

DOI: 10.3389/fgene.2025.1665167

Authors: Xiao Ting Shao, Yu Xuan Dai, Yu Fang Zhao, Yu Hang Chen, Ling Jing Ying

Institution: Jinhua Central Hospital

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $3,801