Clinical phenotype and genetic analysis of a child with CAKUTHED syndrome due to variant of PBX1 gene.
10.3760/cma.j.cn511374-20241015-00535
- Author:
Jiao TANG
1
,
2
;
Chuan ZHANG
;
Ruiqiong YANG
;
Xinyuan TIAN
;
Bingbo ZHOU
;
Yupei WANG
;
Ling HUI
Author Information
1. Department of Clinical Laboratory, the Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 635000, China. hui_lingsfy@
2. com.
- Publication Type:English Abstract
- MeSH:
Humans;
Male;
Pre-B-Cell Leukemia Transcription Factor 1/genetics*;
Phenotype;
Infant, Newborn;
Exome Sequencing;
Mutation, Missense;
Heart Defects, Congenital/genetics*;
Abnormalities, Multiple/genetics*
- From:
Chinese Journal of Medical Genetics
2025;42(12):1471-1476
- CountryChina
- Language:Chinese
-
Abstract:
UNLABELLED:OBJECTIVE：To explore the clinical characteristics and genetic etiology of a child with CAKUTHED syndrome.
METHODS:A child who was admitted to the neonatal department of Gansu Provincial Maternal and Child Health Care Hospital due to "neonatal asphyxia" in May 2021 was selected as the study subject. Genomic DNA was extracted from peripheral venous blood samples from the child and his parents, and whole exome sequencing (WES) was carried out. Sanger sequencing was used to verify the candidate variant of the PBX1 gene. Based on the guidelines from the American College of Medical Genetics and Genomics (ACMG), the pathogenicity of candidate variants was rated. This study was approved by the Medical Ethics Committee of the Hospital [Ethics No.: 2021GSFY (65)].
RESULTS:The proband, a male neonate, manifested renal dysplasia, congenital heart disease, pulmonary dysplasia, mediastinal hernia, cryptorchidism, and clavicle dysplasia. WES revealed that he had harbored a heterozygous c.863G>A (p.Arg288Gln) missense variant in exon 6 of PBX1 gene, which resulted substitution of Arginine at position 288 by Glutamine, for which both parents were of the wild type. The variant was unreported previously and rated as pathogenic (PS2+PM1+PM2_Supporting+PP2+PP3) based on the ACMG guidelines.
CONCLUSION:The c.863G>A variant of the PBX1 gene probably underlay the pathogenesis in the proband. Above finding has enriched the mutational spectrum of the PBX1 gene.
