Genetic analysis of an infant death due to a paternally derived FOXF1 somatic-gonadal mosaic variant.
10.3760/cma.j.cn511374-20230216-00077
- VernacularTitle:父亲
FOXF1基因体细胞-生殖腺嵌合变异导致患儿死亡1例的遗传学分析
- Author:
Jing WANG
1
;
Qingwen ZHU
;
Aiming CUI
;
Mengsi LIN
;
Xian CAO
Author Information
1. The Affiliated Maternity and Child Health Care Hospital of Nantong University, Nantong, Jiangsu 226006, China. ymtnt@sina.com.
- Publication Type:Journal Article
- MeSH:
Female;
Humans;
Pregnancy;
Child;
Infant;
Infant, Newborn;
Male;
Semen;
Infant Death;
Exons;
Mosaicism;
Forkhead Transcription Factors/genetics*
- From:
Chinese Journal of Medical Genetics
2023;40(9):1176-1180
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the genetic characteristics and cause of death for an infant with alveolar capillary dysplasia and pulmonary vein misalignment (ACD/MPV).
METHODS:An infant with ACD/MPV diagnosed at the Affiliated Maternity and Child Health Care Hospital of Nantong University in September 2022 was selected as the study subject. Clinical data of the infant were collected. Whole exome sequencing (WES) was carried out to detect genetic variants in the skin tissue, and Sanger sequencing was performed for verifying the candidate variants in the parents. Droplet digital PCR (ddPCR) was used to determine the mosaicism ratio of the variant in different germ layer-derived samples from the father.
RESULTS:The infant had died within 2 days after birth due to hypoxemia and respiratory distress. WES revealed that she has harbored a c.433C>T nonsense variant in exon 1 of the FOXF1 gene, which was unreported previously. Sanger sequencing has verified the variant in the infant, with her mother's locus being the wild-type and a minor variant peak noted in her father. ddPCR indicated that the mosaic ratio of the c.433C>T variant in the father's sperm was 27.18%, with the mosaic ratios of the variant in tissues originating from the three germ layers ranging from 11% to 28%.
CONCLUSION:The c.433C>T variant derived from the paternal germline and somatic mosaicism of the FOXF1 gene had probably predisposed to the neonatal death of this infant. ddPCR is an effective method for detecting mosaic variants.