Exercise in Marfan syndrome

1Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Diagnosis is made after careful physical examination and echocardiography [7, 19], demonstrating classical features in two out of three major systems (eyes, heart, skeleton), supported by a family history in 75 % of cases [13]. There are many genes which can cause familial thoracic aortic aneurysm and dissection (FTAAD) [16]. If no genetic cause can be found, and aortic measurements are just outside the normal upper limits and are non-progressive, the athlete may be allowed to continue sporting activity with continual echo surveillance.

Cite

CITATION STYLE

APA

Davies, B., & Child, A. H. (2016). Exercise in Marfan syndrome. In Diagnosis and Management of Marfan Syndrome (pp. 263–272). Springer-Verlag London Ltd. https://doi.org/10.1007/978-1-4471-5442-6_24

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free