Extracardiac Manifestations Fail to Predict the Severity of Cardiac Phenotype in Children and Young Adults with Marfan Syndrome

Author:

John Sheba,Young Luciana T.,Lacro Ronald V.,Hoskoppal Arvind,Ou Zhining,Presson Angela P.,Johnson Joyce T.,Andrade Lauren,Minich L. LuAnn,Menon Shaji

Publisher

Springer Science and Business Media LLC

Reference18 articles.

1. Judge DP, Dietz HC (2005) Marfan’s syndrome. Lancet 366:1965–1976

2. Silverman DI, Burton KJ, Gray J, Bosner MS, Douchoukos NT, Roman MJ, Boxer M, Devereux RB, Tsipoura P (1995) Life expectancy in Mafan syndrome. Am J Cardiol 75(2):157–160

3. Baer RW, Taussig HB, Oppenheimer EH (1943) Congenital aneurysmal dilatation of the aorta associated with arachnodactyly. Bull Johns Hopkins Hosp 72:309–331

4. Etter LE, Glover LP (1943) Arachnodactyly complicated by dislocated lens and death from rupture of the dissecting aneurysm aorta. JAMA 123:88–89

5. Hiratzka LF, Bakris GL, Beckman JA et al (2010) ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine [published correction appears in Circulation. 2010 Jul 27;122(4):e410]. Circulation 121(13):e266–e369

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