Analysis of genetic variants and clinical manifestations of two children with Kabuki syndrome.
10.3760/cma.j.cn511374-20220606-00391
- Author:
Yu SHEN
1
;
Shuni SUN
;
Min XIE
;
Haibo LI
;
Limin XU
Author Information
1. Department of Perinatology, Ningbo Women and Children's Hospital, Ningbo, Zhejiang 315012, China. xuliminbaby@163.com.
- Publication Type:Journal Article
- MeSH:
Child;
Female;
Humans;
Abnormalities, Multiple/genetics*;
Intellectual Disability/genetics*;
Genetic Counseling;
Genetic Testing;
Mutation
- From:
Chinese Journal of Medical Genetics
2023;40(7):833-837
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To report on two children with Kabuki syndrome due to variants of the KMT2D gene and summarize their clinical and genetic characteristics.
METHODS:Two children who had presented at the Ningbo Women and Children's Hospital respectively on August 19 and November 10, 2021 were selected as the study subjects. Clinical data were collected. Both children were subjected to whole exome sequencing (WES), and candidate variants were validated by Sanger sequencing.
RESULTS:Both children had featured motor and language developmental delay, facial dysmorphism and mental retardation. Genetic testing revealed that both had harbored de novo heterozygous variants of the KMT2D gene, namely c.10205del (p.Leu3402Argfs*3) and c.5104C>T (p.Arg1702*), both of which were rated as pathogenic variants based on the guidelines from the American College of Medical Genetics and Genomics (ACMG).
CONCLUSION:The c.10205del (p.Leu3402Argfs*3) and c.5104C>T (p.Arg1702*) variants of the KMT2D gene probably underlay the pathogenesis in these two children. Above finding has not only provided a basis for their diagnosis and genetic counseling, but also enriched the spectrum of KMT2D gene variants.
