Literature DB >> 1785300

Idiopathic dilatation of the aorta with dissection in a family without Marfan syndrome.

D Teien1, J P Finley, D A Murphy, A Lacson, J Longhi, D A Gillis.   

Abstract

Dissection of the aorta is very rare in children, but classically occurs in the presence of Marfan syndrome or other connective tissue disorder. We present a case of spontaneous dissection in a 12-year-old boy whose half brother has an idiopathic dilated aorta and whose mother has also required surgery for dissection of a dilated aorta. No features of connective tissue disorder were present in any family member.

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Year:  1991        PMID: 1785300     DOI: 10.1111/j.1651-2227.1991.tb11818.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  3 in total

1.  Aortic dissection and rupture in an 11-year-old child: A case report.

Authors:  Lucy Youngmin Eun; Deok Kyu Cho; Yun Hyeong Cho; Ki Hyun Byun
Journal:  J Cardiol Cases       Date:  2010-10-15

2.  Aortic dissection and rupture in a child.

Authors:  Yun Ju Jo; Eun Jeong Lee; Jin Won Oh; Chang Min Moon; Deok Kyu Cho; Yun Hyeong Cho; Ki Hyun Byun; Lucy Youngmin Eun
Journal:  Korean Circ J       Date:  2011-03-31       Impact factor: 3.243

Review 3.  Patent arterial duct.

Authors:  Jonathan T Forsey; Ola A Elmasry; Robin P Martin
Journal:  Orphanet J Rare Dis       Date:  2009-07-10       Impact factor: 4.123

  3 in total

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