Clinical and genetic analysis of two children with intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia.
10.3760/cma.j.cn511374-20220402-00224
- Author:
Na QI
1
;
Ke YANG
;
Xingxing LEI
;
Fengyang WANG
;
Dong WU
;
Yue GAO
;
Yuwei ZHANG
;
Shixiu LIAO
Author Information
1. Institute of Medical Genetics, Henan Provincial People's Hospital, Zhengzhou, Henan 450003, China. ychslshx@126.com.
- Publication Type:Journal Article
- MeSH:
Humans;
Child;
Female;
Child, Preschool;
Microcephaly/genetics*;
Developmental Disabilities/genetics*;
Intellectual Disability/complications*;
Comparative Genomic Hybridization;
Mutation
- From:
Chinese Journal of Medical Genetics
2023;40(4):408-412
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical features and genetic etiology of two children with intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia (MICPCH).
METHODS:Two children with MICPCH who were presented at the Henan Provincial People's Hospital between April 2019 and December 2021 were selected as the study subjects. Clinical data of the two children were collected, along with peripheral venous blood samples of them and their parents, and amniotic fluid sample of the mother of child 1. Whole exome sequencing (WES), array-comparative genomic hybridization (aCGH) and real-time quantitative PCR (qPCR) were carried out for the children, their parents and the fetus. The pathogenicity of candidate variants were evaluated.
RESULTS:Child 1 was a 6-year-old girl featuring motor and language delay, whilst child 2 was a 4.5-year-old girl mainly featuring microcephaly and mental retardation. WES revealed that child 2 has harbored a 158.7 kb duplication in Xp11.4 (chrX: 41446160_41604854), which has encompassed exons 4~14 of the CASK gene. The same duplication was not found in either of her parents. aCGH revealed that child 1 has harbored a 29 kb deletion at Xp11.4 (chrX: 41637892_41666665), which encompassed exon 3 of the CASK gene. The same deletion was not found in either of her parents and the fetus. The above results were confirmed by qPCR assay. Above deletion and duplication were not found in the ExAC, 1000 Genomes and gnomAD databases. Based on the guidelines from the American College of Medical Genetics and Genomics (ACMG), both variants were rated as likely pathogenic (PS2+PM2_Supporting).
CONCLUSION:The deletion of exon 3 and duplication of exons 4~14 of the CASK gene probably underlay the pathogenesis of MICPCH in these two children, respectively.
