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.
CITATION STYLE
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
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