Back to Search Start Over

Inherited Disorders of Connective Tissue.

Authors :
Willerson, James T.
Wellens, Hein J. J.
Cohn, Jay N.
Holmes, David R.
Milewicz, Dianna M.
Source :
Cardiovascular Medicine; 2007, p2557-2565, 9p
Publication Year :
2007

Abstract

Marfan syndrome is an autosomal dominant disease characterized by pleiotropic manifestations involving the cardiovascular, ocular, and skeletal systems. The most common cardiovascular complication in patients with Marfan syndrome is progressive aortic root enlargement initially occurring at the sinuses of Valsalva. Some patients have dissections of the aorta, most often a type I dissection. Mitral valve prolapse is very common in these patients.The majority of patients with thoracic aortic aneurysms and dissections who have cystic medial necrosis of the aorta do not have Marfan syndrome.Ehlers-Danlos syndrome (EDS) is a heterogeneous group of disorders that are classified together on the basis of skin hyperextensibility, cutaneous fragility, joint laxity, dystrophic scarring, and easy bruising. Spontaneous arterial rupture occurs in type IV EDS.Supravalvular aortic stenosis is an autosomal dominant disorder caused by narrowing of the ascending aorta just distal to the coronary ostia.Pseudoxanthoma elasticum is an inherited disease caused by progressive calcification of elastic fibers in the connective tissue throughout the body. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISBNs :
9781846281884
Database :
Complementary Index
Journal :
Cardiovascular Medicine
Publication Type :
Book
Accession number :
34136072
Full Text :
https://doi.org/10.1007/978-1-84628-715-2_124