{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,4,19]],"date-time":"2025-04-19T08:49:29Z","timestamp":1745052569725},"reference-count":13,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2014,2,6]],"date-time":"2014-02-06T00:00:00Z","timestamp":1391644800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Forensic Sciences"],"published-print":{"date-parts":[[2014,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Marfan syndrome is an autosomal dominant genetic disorder of the connective tissue. The most serious complications of this syndrome are defects of the heart valves and aorta. Aneurysms of thoracic aorta are known to develop in Marfan syndrome. Other causes for development of aneurysms of the thoracic aorta are trauma, infections, valve and arch anomalies, genetic disorders, and atherosclerosis. These aneurysms upon rupture may lead to sudden deaths. They are usually detected during routine screening or follow\u2010up of such persons suffering from Marfan syndrome and upon death will be certified by the treating physician. Thus, an autopsy surgeon rarely comes across such deaths. One such case of sudden death due to cardiac tamponade consequent upon rupture of dissecting aortic aneurysm in a 33\u2010year\u2010old male who complained of throbbing pains in the chest, radiating to back, became breathless, cyanotic and died on the way to hospital is being presented here.<\/jats:p>","DOI":"10.1111\/1556-4029.12415","type":"journal-article","created":{"date-parts":[[2014,2,6]],"date-time":"2014-02-06T22:46:48Z","timestamp":1391726808000},"page":"1126-1128","source":"Crossref","is-referenced-by-count":11,"title":["Sudden Death in Marfan Syndrome"],"prefix":"10.1111","volume":"59","author":[{"given":"Basappa S.","family":"Hugar","sequence":"first","affiliation":[{"name":"Department of Forensic Medicine MS Ramaiah Medical College Bangalore 560054 India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shivaramareddy","family":"Praveen","sequence":"additional","affiliation":[{"name":"Department of Forensic Medicine MS Ramaiah Medical College Bangalore 560054 India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sunil K.","family":"Kainoor","sequence":"additional","affiliation":[{"name":"Department of Forensic Medicine MS Ramaiah Medical College Bangalore 560054 India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Akshith Raj S.","family":"Shetty","sequence":"additional","affiliation":[{"name":"Department of Forensic Medicine MS Ramaiah Medical College Bangalore 560054 India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,2,6]]},"reference":[{"key":"e_1_2_5_2_1","unstructured":"MarfanA.A case of congenital deformation of the four limbs more pronounced at the extremities characterized by elongation of the bones with some degree of thinning. Bulletins et memoires de la Soci\u00e9t\u00e9medicale des h\u00f4spitaux de Paris.1896;13(3rd series):220\u20136."},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1038\/352337a0"},{"key":"e_1_2_5_4_1","article-title":"Marfan syndrome linked to gene","author":"Brown P","year":"1991","journal-title":"New Scientist. 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