Analysis of a case of Multiple pterygium syndrome due to a novel variant of CHRNG gene.
10.3760/cma.j.cn511374-20220107-00009
- Author:
Yiru CHEN
1
;
Tianying NONG
;
Weizhe SHI
;
Jiangui LI
;
Xuejiao DING
;
Yue LI
;
Mingwei ZHU
;
Hongwen XU
Author Information
1. Guangzhou Women and Children's Medical Center Affiliated to Guangzhou Medical University, Guangzhou, Guangdong 510630, China. mingwei.zhu@gwcmc.org.
- Publication Type:Journal Article
- MeSH:
Humans;
Child;
Female;
Abnormalities, Multiple/genetics*;
Malignant Hyperthermia/genetics*;
Skin Abnormalities/genetics*;
Heterozygote;
Mutation;
Receptors, Nicotinic/genetics*
- From:
Chinese Journal of Medical Genetics
2023;40(6):686-690
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical characteristics and genetic etiology of a child with multiple pterygium syndrome (MPS).
METHODS:A child with MPS who was treated at the Orthopedics Department of Guangzhou Women and Children's Medical Center Affiliated to Guangzhou Medical University on August 19, 2020 was selected as the study subject. Clinical data of the child was collected. Peripheral blood samples of the child and her parents were also collected. Whole exome sequencing (WES) was carried out for the child. Candidate variant was validated by Sanger sequencing of her parents and bioinformatic analysis.
RESULTS:The child, an 11-year-old female, had a complain of "scoliosis found 8 years before and aggravated with unequal shoulder height for 1 year". WES results revealed that she has carried a homozygous c.55+1G>C splice variant of the CHRNG gene, for which both of her parents were heterozygous carriers. By bioinformatic analysis, the c.55+1G>C variant has not been recorded by the CNKI, Wanfang data knowledge service platform and HGMG databases. Analysis with Multain online software suggested that the amino acid encoded by this site is highly conserved among various species. As predicted with the CRYP-SKIP online software, the probability of activation and skipping of the potential splice site in exon 1 caused by this variant is 0.30 and 0.70, respectively. The child was diagnosed with MPS.
CONCLUSION:The CHRNG gene c.55+1G>C variant probably underlay the MPS in this patient.
