Clinical phenotypes and genetic analysis of five children with Lamb-Shaffer syndrome due to novel variants of SOX5 gene.
10.3760/cma.j.cn511374-20251011-00593
- Author:
Ziyan ZHANG
1
,
2
;
Yaxue XIE
;
Ping PANG
;
Qiyan LIU
;
Zhichao LI
;
Guang YANG
Author Information
1. Department of Pediatric Medicine, Chinese PLA General Hospital, Beijing 100700, China. yangg301@
2. com.
- Publication Type:Journal Article
- MeSH:
Humans;
Male;
Female;
Phenotype;
Child, Preschool;
Child;
SOXD Transcription Factors/genetics*;
Exome Sequencing;
Mutation;
Infant
- From:
Chinese Journal of Medical Genetics
2026;43(1):13-18
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical phenotypes and genetic characteristics of five children with Lamb-Shaffer syndrome (LAMSHF).
METHODS:Five children with LAMSHF diagnosed at the Department of Pediatrics, the First Medical Center of Chinese PLA General Hospital from April 2021 to December 2024 were selected as study subjects. Clinical data of the children was collected. Genomic DNA was extracted from peripheral blood samples of the children and their parents. Whole exome sequencing (WES) was carried out to screen for variants. This study was approved by the Medical Ethics Committee of the Chinese PLA General Hospital (Ethics No.: S2025-411-01).
RESULTS:All five children had presented with global developmental delay. Among them, two had manifestations of autism spectrum disorder, two had abnormal electroencephalogram findings, four had abnormal MRI results, and two had ocular abnormalities. WES has detected five novel variants in the SOX5 gene. Among these, c.1771G>C (p.Gly591Arg) was unreported previously. Sanger sequencing confirmed that none of the parents had carried the same variants, suggesting that they were all de novo variants. According to the guidelines from the American College of Medical Genetics and Genomics (ACMG), two nonsense variants and one missense variant were classified as pathogenic, whilst two missense variants were classified as likely pathogenic.
CONCLUSION:This study has clarified the correlation between the clinical phenotypes of five children with LAMSHF and variants of the SOX5 gene, which expanded the mutational spectrum of the SOX5 gene and provided a basis for the clinical diagnosis and genetic counseling.
