Two cases of female-restricted X-linked syndromic mental retardation-99 caused by USP9X gene variations
10.3760/cma.j.cn101070-20201012-01605
- VernacularTitle:USP9X基因变异致限于女性型X-连锁综合征型智力障碍99型2例
- Author:
Wenxin ZHANG
1
;
Dalin FU
;
Chunli WANG
;
Ling ZHANG
;
Xiaoke ZHAO
Author Information
1. 南京医科大学附属儿童医院康复医学科 210008
- Keywords:
Intellectual disability;
USP9 X gene;
Female-restricted X-linked syndromic mental retardation-99
- From:
Chinese Journal of Applied Clinical Pediatrics
2021;36(23):1824-1827
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To summarize and analyze the clinical and genotype features of female-restricted X-linked syndromic mental retardation-99(MRXS99F, OMIM: 300968)caused by USP9 X gene mutation, and to improve the clinicians′ understanding of the disease. Methods:Clinical data and genotypes of 2 children with MRXS99F treated in the Children′s Hospital of Nanjing Medical University in March 2020 (case 1) and June 2020 (case 2) were analyzed, and the relevant databases at home and abroad were reviewed to summarize the clinical characteristics and gene variation characteristics of the disease.Results:The 2 cases were 6 months old (case 1) and 5 years old (case 2), both showed psychomotor retardation.Case 1 presented a short stature, pigment abnormality, characteristic facial features, hypotonia, recurrent respiratory tract infections, laryngeal cartilage hypoplasia, atrial septal defect, feeding difficulty, hearing loss and brain hypoplasia.Case 2 had abnormal electroencephalogram.As confirmed by whole-exome sequencing, two children carried c. 6972+ 1G>A, c.6437C>T of USP9 X, respectively.Neither of the 2 variations was previously reported.Twenty-two cases of MRXS99F caused by USP9 X gene mutation were reported in 4 literatures globally, and 24 cases were combined with this study.The clinical manifestations of 20/22 children had special faces.All of them accompanied mental retardation combined with motor and language retardation, and carried neonatal variation. Conclusions:This is the first case report of MRXS99F induced by USP9 X gene variation in China.MRXS99F caused by functional deletion and variation of USP9 X gene is mainly characterized by psychomotor retardation, language disorder, special face and multiple congenital malformations.For children with unexplained growth retardation, special face and multiple congenital malformations, genetic testing like high-throughput sequencing should be carried out as early as possible to determine the etiology.
