Clinical and genetic analysis of a patient with 10q26.3 microdeletion in conjunct with 18q22.3q23 microduplication.
10.3760/cma.j.cn511374-20211126-00943
- Author:
Jianlong ZHUANG
1
;
Shuhong ZENG
;
Yuanbai WANG
;
Yuying JIANG
Author Information
1. Center for Prenatal Diagnosis, Quanzhou Women's and Children's Hospital, Quanzhou, Fujian 362000, China. 1287194067@qq.com.
- Publication Type:Journal Article
- MeSH:
Female;
Animals;
Genetic Testing;
Genetic Counseling;
Karyotyping;
Chromosome Banding;
Genomics
- From:
Chinese Journal of Medical Genetics
2022;39(12):1415-1418
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic etiology for a patient featuring intellectual disability and torticollis.
METHODS:Peripheral blood sample was collected from the patient and subjected to G-banded karyotyping analysis and single nucleotide polymorphism array (SNP-array) assay.
RESULTS:The patient was found to have a chromosomal karyotype of 46,XX. SNP-array revealed that she has harbored a 3.8 Mb microdeletion at 10q26.3 which has encompassed 21 OMIM genes including EBF3 and ECHS1, and a 7.3 Mb duplication at 18q22.3q23 which has encompassed 19 OMIM genes including TSHZ1 and TXNL4A. Based on the guidelines from the American College of Medical Genetics and Genomics (ACMG), the 10q26.3 deletion was predicted to be pathogenic, whilst the 18q22.3q23 duplication was predicted to be variation of unknown significance.
CONCLUSION:The clinical phenotype of the patient may be mainly attributed to the 10q26.3 microdeletion, and haploinsufficiency of the EBF3 gene may account for her intellectual deficiency. Above finding has provided a basis for genetic counseling for the patient.
