Analysis of the pedigree of a child with interstitial lung disease caused by a novel mutation of p. K114N in SFTPC gene
10.3760/cma.j.issn.1673-4912.2021.06.010
- VernacularTitle:SFTPC基因p.K114N新发突变致儿童间质性肺疾病一家系分析
- Author:
Xiaojun DUAN
1
;
Xi ZHANG
;
Yanni MENG
;
Jin ZHANG
;
Linrui LI
;
Xuan SHI
;
Lu CHEN
;
Yanping CHEN
Author Information
1. 湖南省儿童医院呼吸内科，长沙 410007
- Keywords:
Interstitial lung disease;
Children;
Surfactant protein C;
Gene;
Novel mutation
- From:
Chinese Pediatric Emergency Medicine
2021;28(6):487-491
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To analyze the clinical and chest CT features in a family with interstitial lung disease(ILD), and assess the probable causative gene mutations for the family.Methods:In order to identify the etiology of the proband′s ILD, the pedigree was investigated.The clinical data of five proband′s pedigree members were collected, and the chest HRCT examination was performed on four proband′s pedigree members with respiratory symptoms.The human whole exon sequencing was performed on the proband′s blood samples, then its deleterious effects were assessed.Subsequently, the strong pathogenic mutation was validated by Sanger sequencing.Results:According to the family survey, there were five patients with ILD in the family, including three males and two females.One of them died.The surfactant protein C(SFTPC)gene(exon4, c.342G>T, p.K114N)was found in all four surviving patients.The mutation was considered to be originated from the father of the proband, and the pathogenic mutation was considered, which was not included in the databases and was a noval mutation.In addition, the clinical manifestations of different patients in the family were significantly different.Conclusion:The novel mutation of p. k114n in SFTPC gene can lead to ILD in children, and the mutation has incomplete exons in family members.Chest CT and whole exon sequencing play an important role in the diagnosis of ILD in children.
