Authors
Michael Silberbach, Jolien W Roos-Hesselink, Niels H Andersen, Alan C Braverman, Nicole Brown, R Thomas Collins, Julie De Backer, Kim A Eagle, Loren F Hiratzka, Walter H Johnson Jr, Daniella Kadian-Dodov, Leo Lopez, Kristian H Mortensen, Siddharth K Prakash, Elizabeth V Ratchford, Arwa Saidi, Iris van Hagen, Luciana T Young, American Heart Association Council on Cardiovascular Disease in the Young; Council on Genomic and Precision Medicine; and Council on Peripheral Vascular Disease
Publication date
2018/10
Source
Circulation: Genomic and precision medicine
Volume
11
Issue
10
Pages
e000048
Publisher
Lippincott Williams & Wilkins
Description
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 …
Total citations
2018201920202021202220232024192128354332
Scholar articles
M Silberbach, JW Roos-Hesselink, NH Andersen… - Circulation: Genomic and precision medicine, 2018