Fatigue in patients with syndromic heritable thoracic aortic disease: a systematic review of the literature and a qualitative study of patients’ experiences and perceptions

[1] Monda E(2023)The role of genetic testing in patients with heritable thoracic aortic diseases Diagnostics 13 772-594

[2] Lioncino M(2022)Guideline for the diagnosis and management of aortic disease: a report of the American heart association/American college of cardiology joint committee on clinical practice guidelines Circulation 6 582-20

[3] Verrillo F(2021)American Heart Association Council on Genomic and Precision Medicine; Council on Lifelong Congenital Heart Disease and Heart Health in the Young; Council on Arteriosclerosis, Thrombosis and Vascular Biology; and Council on Lifestyle and Cardiometabolic Health. Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association Circ Genom Precis Med 5 11-615

[4] Rubino M(2017)Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome Ann Cardiothorac Surg 72 605-79

[5] Caiazza M(2017)Genes associated with thoracic aortic aneurysm and dissection: an update and clinical implications Aorta 12 63-99

[6] Mauriello A(2018)Clinical validity of genes for heritable thoracic aortic aneurysm and dissection J Am Coll Cardiol 32 86-535

[7] Isselbacher EM(2022)Genetics of heritable thoracic aortic disease (Review) Cardiogenetics 3 526-266

[8] Preventza O(2016)The expanding clinical spectrum of extra cardiovascular and cardiovascular manifestations of heritable thoracic aortic aneurysm and dissection Can J Cardiol 17 251-1975

[9] Black HJ(2020)Marfan syndrome and exercise: a literature review Trans Sport Med 44 1968-2471

[10] Augoustides JG(2019)Exercise and sports participation in patients with thoracic aortic disease: a review Expert Rev Cardiovasc Ther 43 2464-915

[1] Monda E(2023)The role of genetic testing in patients with heritable thoracic aortic diseases Diagnostics 13 772-594

[2] Lioncino M(2022)Guideline for the diagnosis and management of aortic disease: a report of the American heart association/American college of cardiology joint committee on clinical practice guidelines Circulation 6 582-20

[3] Verrillo F(2021)American Heart Association Council on Genomic and Precision Medicine; Council on Lifelong Congenital Heart Disease and Heart Health in the Young; Council on Arteriosclerosis, Thrombosis and Vascular Biology; and Council on Lifestyle and Cardiometabolic Health. Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association Circ Genom Precis Med 5 11-615

[4] Rubino M(2017)Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome Ann Cardiothorac Surg 72 605-79

[5] Caiazza M(2017)Genes associated with thoracic aortic aneurysm and dissection: an update and clinical implications Aorta 12 63-99

[6] Mauriello A(2018)Clinical validity of genes for heritable thoracic aortic aneurysm and dissection J Am Coll Cardiol 32 86-535

[7] Isselbacher EM(2022)Genetics of heritable thoracic aortic disease (Review) Cardiogenetics 3 526-266

[8] Preventza O(2016)The expanding clinical spectrum of extra cardiovascular and cardiovascular manifestations of heritable thoracic aortic aneurysm and dissection Can J Cardiol 17 251-1975

[9] Black HJ(2020)Marfan syndrome and exercise: a literature review Trans Sport Med 44 1968-2471

[10] Augoustides JG(2019)Exercise and sports participation in patients with thoracic aortic disease: a review Expert Rev Cardiovasc Ther 43 2464-915