Advances in cardiovascular diseases in children with Turner syndrome
10.3760/cma.j.issn.1673-4408.2024.02.009
- VernacularTitle:特纳综合征患儿心血管疾病研究进展
- Author:
Feihan HU
1
;
Yirou WANG
;
Xiumin WANG
Author Information
1. 上海交通大学医学院附属上海儿童医学中心内分泌遗传代谢科 200127
- Keywords:
Turner syndrome;
Bicuspid aortic valve;
Aortic dilatation;
Aortic dissection
- From:
International Journal of Pediatrics
2024;51(2):107-110
- CountryChina
- Language:Chinese
-
Abstract:
Turner syndrome(TS),a condition among females with a karyotype containing one X chromosome and complete or partial absence of the second sex chromosome,affects 20~50 in 100 000 newborn girls. Congenital or acquired cardiovascular diseases are present in about half of patients with TS. The congenital defects occur in about 25%~50% of TS patients;aortic dilatation as an important risk factor for aortic dissection is common in adult patients with TS. Furthermore,arrhythmias are found more frequently in patients with TS. A higher prevalence of hypertension in children and adolescents with TS has also been reported,and the application of 24h ambulatory blood pressure monitoring may facilitates the diagnosis of hypertension among these children and adolescent.Thus,active health education,correct follow-up and timely intervention are crucially needed.