Circ Genom Precis Med. 2018 Oct;11(10):e000048. doi: 10.1161/HCG.0000000000000048.
Girls and women with Turner syndrome face a lifelong struggle with both congenital heart disease and acquired cardiovascular conditions. Bicuspid aortic valve is common, and many have left-sided heart obstructive disease of varying severity, from hypoplastic left-sided heart syndrome to minimal aortic stenosis or coarctation of the aorta. Significant enlargement of the thoracic aorta may progress to catastrophic aortic dissection and rupture. It is becoming increasingly apparent that a variety of other cardiovascular conditions, including early-onset hypertension, ischemic heart disease, and stroke, are the major factors reducing the life span of those with Turner syndrome. The presentations and management of cardiovascular conditions in Turner syndrome differ significantly from the general population. Therefore, an international working group reviewed the available evidence regarding the diagnosis and treatment of cardiovascular diseases in Turner syndrome. It is recognized that the suggestions for clinical practice stated here are only the beginning of a process that must also involve the establishment of quality indicators, structures and processes for implementation, and outcome studies.
特纳综合征女孩和妇女面临着先天性心脏病和后天性心血管疾病的终身斗争。二叶式主动脉瓣很常见,许多人有不同严重程度的左侧心腔阻塞性疾病,从左心发育不全综合征到轻微主动脉瓣狭窄或主动脉缩窄。胸主动脉的显著增大可能进展为灾难性主动脉夹层和破裂。越来越明显的是,各种其他心血管疾病,包括早发性高血压、缺血性心脏病和中风,是降低特纳综合征患者寿命的主要因素。特纳综合征中心血管疾病的表现和管理与一般人群明显不同。因此,一个国际工作组审查了有关特纳综合征中心血管疾病的诊断和治疗的现有证据。这里提出的临床实践建议仅仅是一个过程的开始,这个过程还必须包括建立质量指标、实施的结构和流程,以及结果研究。