Open AccessMarfan Syndrome: A Report of Two Cases and Review
Author(s) -
Vinay Kumar Reddy K,
Venkata Satya Ramesh T,
Dornadula Koteeswaran,
M Jayakiran,
Sivaranjani Yeluri,
S Kailasam
Publication year - 2011
Publication title -
journal of indian academy of oral medicine and radiology
Language(s) - English
Resource type - Journals
eISSN - 0975-1572
pISSN - 0972-1363
DOI - 10.5005/jp-journals-10011-1139
Subject(s) - medicine , marfan syndrome , intensive care medicine , pediatrics , general surgery , surgery
Marfan syndrome is an autosomal dominant disorder of the connective tissues, resulting in abnormalities of the musculoskeletal system, cardiovascular system and eyes. It has a prevalence of 1 in 100,000 population and occurs in all ethnic groups. It may be familial or due to new mutation (30%), in the fibrillin gene on arm of chromosome 15. It is estimated that one person in every 3000 to 5000 has Marfan′s syndrome may have cardiovascular abnormalities and may be complicated by infective endocarditis. About 90% of Marfan patients will develop cardiac complications