Clinical and genetic analysis of two cases with Rubinstein-Taybi syndrome.
10.3760/cma.j.issn.1003-9406.2019.09.008
- VernacularTitle:两例Rubinstein-Taybi综合征患儿的临床及遗传学分析
- Author:
Fang TANG
1
;
Zhonghui LI
;
Xinran CHENG
;
Na SU
;
Li YAN
;
Peng GOU
;
Chunzhu GONG
Author Information
1. The Affiliated Hospital, School of Medicine, UESTC, Chengdu Women's and Children's Central Hospital, Chengdu, Sichuan 610019, China.cxr1216@sina.com.
- Publication Type:Journal Article
- MeSH:
CREB-Binding Protein;
genetics;
Genetic Testing;
High-Throughput Nucleotide Sequencing;
Humans;
Phenotype;
Rubinstein-Taybi Syndrome;
genetics
- From:
Chinese Journal of Medical Genetics
2019;36(9):886-889
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To summarize the clinical characteristics and identify gene mutations of 2 probands with Rubinstein-Taybi syndrome (RSTS).
METHODS:Clinical characteristics of 2 probands with Rubinstein-Taybi syndrome were summarized. Genomic DNA was extracted from peripheral blood samples from the patients and their parents. Genomic DNA was subjected to whole exome next generation sequencing. Suspected variants were confirmed by Sanger sequencing.
RESULTS:The two patients were characterized by typical facial features, broad thumbs and big toes, intellectual disability, and postnatal growth retardation. Two variants of the CREBBP gene, namely c.3779+1G>A and c.5052_c.5053insT, were respectively identified in the 2 patients. Among these, c.3779+1G>A was a previously known pathological mutation, while c.5052_c.5053insT was unreported previously. Both variants were predicted to be pathological.
CONCLUSION:Two cases of Rubinstein-Taybi syndrome were diagnosed, which facilitated the diagnosis and genetic counselling.
