Genetic analysis of a child with Oculo-facio-cardio-dental syndrome due to a deletional variant of BCOR gene.
10.3760/cma.j.cn511374-20250728-00461
- Author:
Rui TANG
1
;
Yuan YANG
;
Yunqiang LIU
Author Information
1. Department of Medical Genetics, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China. yq_liu@scu.edu.cn.
- Publication Type:English Abstract
- MeSH:
Humans;
Male;
Repressor Proteins/genetics*;
Proto-Oncogene Proteins/genetics*;
Tooth Abnormalities/genetics*;
Eye Abnormalities/genetics*;
Microphthalmos/genetics*;
Child;
Sequence Deletion;
Female;
Cataract/congenital*;
Heart Septal Defects
- From:
Chinese Journal of Medical Genetics
2025;42(11):1364-1368
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic etiology of a Chinese boy affected with Oculo-facio-cardio-dental syndrome (OFCD).
METHODS:A child diagnosed with OFCD at West China Hospital of Sichuan University on September 21, 2024 was selected as the study subject. Clinical phenotype of the child was collected through ophthalmologic examination, cardiac ultrasonography, and X-ray imaging. Potential pathogenic variants were detected by trio-whole exome sequencing (Trio-WES). Candidate variant was validated with TA-cloning followed by Sanger sequencing. Mosaic variant was analyzed by ultra-deep sequencing (10,000-fold) and quantitative PCR. This study was approved by the Medical Ethics Committee of the West China Hospital of Sichuan University (Ethics No.: 2019-772 ).
RESULTS:The proband had presented with congenital cataracts, mitosis, atrial and ventricular septal defects, dental abnormalities, and right radioulnar synostosis. His mother also exhibited congenital cataracts and dental anomalies, suggesting a diagnosis of OFCD. Trio-WES revealed an novel heterozygous 14-bp deletion (c.4724_4737del) in exon 12 of the BCOR gene in the proband. Deep sequencing identified a mosaic BCOR c.4724_4737del mutation in approximately 3.4% of peripheral leukocytes from his mother. Quantitative PCR analysis also confirmed the presence of this low-level mosaicism. The 14-bp deletion was predicted to cause a frame shift and premature termination (p.Met1575AsnfsTer6). Based on the guidelines from the American College of Medical Genetics and Genomics (ACMG), the variant was classified as pathogenic (PVS1+PM2+PP1).
CONCLUSION:Above findings have expanded the spectrum of BCOR mutations associated with OFCD, which highlighted the role of low-level mosaicism with maternal transmission and provided a basis for genetic counseling and reproductive guidance for the family.
