Analysis of a child with Osteo-oto-hepato-enteric syndrome and a literature review.
10.3760/cma.j.cn511374-20250912-00542
- Author:
Dandan WANG
1
,
2
;
Qianqian LI
;
Hongxiang GUO
;
Yongning CHEN
;
Qingfei HAO
;
Yanlei XU
;
Xiuyong CHENG
Author Information
1. Department of Neonatology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China. chengxy188@
2. com.
- Publication Type:English Abstract
- MeSH:
Humans;
Female;
Infant, Newborn;
Male;
Mutation;
Hearing Loss, Sensorineural/genetics*;
Diarrhea, Infantile/genetics*;
Exome Sequencing;
Phenotype;
Fetal Growth Retardation;
Hair Diseases;
Facies
- From:
Chinese Journal of Medical Genetics
2026;43(3):204-212
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To analyze the phenotype and genotype of a neonate with Osteo-oto-hepato-enteric syndrome (O2HE) and review the literature.
METHODS:A female neonate diagnosed with O2HE syndrome on December 13, 2024 at the First Affiliated Hospital of Zhengzhou University was selected as the study subject, and her clinical characteristics were analyzed, and pathogenic variants were explored by whole exome sequencing (WES). This study was approved by the Medical Ethics Committee of the Hospital (Ethics No.: 2025-KY-1038).
RESULTS:The proband, a female infant, was delivered by Cesarean section at 36+1 weeks of gestation. Five days after birth, she had developed severe diarrhea, mild cholestasis, sensorineural hearing loss, and growth retardation. WES revealed that she has harbored novel compound heterozygous variants c.512delA (p.Lys171Serfs*64) and c.698C>A (p.Thr233Asn) of the UNC45A gene, which were inherited from her mother and father, respectively. A total of 8 English papers were retrieved, which involved 16 patients from 14 families. Combined with our case, the 17 patients included 13 (76.5%) females and 4 (23.5%) males. Four patients (23.5%) had consanguineous parents. One case was excluded from further genetic analysis due to co-morbidity with other genetic variants. The primary clinical features included diarrhea (87.5%), cholestasis (81.3%), sensorineural hearing loss (31.3%), bone fragility (37.5%), and developmental delay (50.0%). Bi-allelic compound heterozygous mutations were identified in 12 patients (75.0%), and homozygous variants in 4 (25.0%). These included missense, nonsense, frameshift and deletional variants. The c.710T>C (p.Leu237Pro) variant was identified for 5 times, 3 of which were in homozygote forms.
CONCLUSION:O2HE syndrome should be suspected in cases with diarrhea, cholestasis, and hearing abnormalities during early postnatal period. Genetic testing facilitate early identification, genetic diagnosis and treatment.
