Genetic analysis of a child with Kartagener syndrome due to novel compound heterozygous variants of DNAH5 gene.
10.3760/cma.j.cn511374-20220110-00020
- Author:
Shan ZHANG
1
;
Chaobing WANG
;
Yong ZHANG
;
Yandong HU
;
Xu LI
;
Chuang ZHI
Author Information
1. Department of Pediatrics, Qionglai Maternal and Child Health Care Hospital, Qionglai, Sichuan 611530, China. zhangshan2022@163.com.
- Publication Type:Journal Article
- MeSH:
Male;
Humans;
Child;
Mutation;
Kartagener Syndrome/genetics*;
Genetic Testing;
Mutation, Missense;
Exome Sequencing;
Axonemal Dyneins/genetics*
- From:
Chinese Journal of Medical Genetics
2023;40(1):71-75
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical characteristics and genetic basis of a child with Kartagener syndrome (KTS).
METHODS:Trio-whole exome sequencing was carried out for the child and his parents, and candidate variants were verified by Sanger sequencing. Changes in protein structure due to missense variants were simulated and analyzed, and the Human Splicing Finder 3.0 (HSF 3.0) online platform was used to predict the effect of the variant of the non-coding region.
RESULTS:The child had featured bronchiectasis, sinusitis and visceral inversion. Genetic testing revealed that he has harbored compound heterozygous variants of the DNAH5 gene, namely c.5174T>C and c.7610-3T>G. Sanger sequencing confirmed the existence of the variants. The variants were not found in the dbSNP, 1000 Genomes, ExAC, ClinVar and HGMD databases. Protein structural analysis suggested that the c.5174T>C (p.Leu1725Pro) variant may affect the stability of local structure and its biological activity. The results of HSF 3.0 analysis suggested that the c.7610-3T>G variant has probably destroyed a splicing receptor to affect the transcription process.
CONCLUSION:The compound heterozygous variants of the DNAH5 gene probably underlay the pathogenesis in the child. Above finding may facilitate the understanding of the clinical characteristics and genetic basis of KTS, and further expand the spectrum of DNAH5 gene variants.
