Pathophysiology and Management of Cardiovascular Manifestations in Marfan and Loeys

Pathophysiology and Management of Cardiovascular Manifestations in Marfan and Loeys–Dietz Syndromes

Published:2016 Issue:3 Volume:57 Page:271-277
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Takeda Norifumi¹,Yagi Hiroki¹,Hara Hironori¹,Fujiwara Takayuki¹,Fujita Daishi¹,Nawata Kan²,Inuzuka Ryo³,Taniguchi Yuki⁴,Harada Mutsuo¹,Toko Haruhiro¹,Akazawa Hiroshi¹,Komuro Issei¹

Affiliation:

1. Department of Cardiovascular Medicine, The University of Tokyo Hospital

2. Department of Cardiovascular Surgery, The University of Tokyo Hospital

3. Department of Pediatrics, The University of Tokyo Hospital

4. Department of Orthopedic Surgery, The University of Tokyo Hospital

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/ihj/57/3/57_16-094/_pdf

Reference83 articles.

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2. 2. Baer RW, Taussig HB, Oppenheimer EH. Congenital aneurysmal dilatation of the aorta associated with arachnodactyly. Bull Johns Hopkins Hosp 1943; 72: 309-31.

3. 3. Etter LE, Glover LP. Arachnodactyly complicated by dislocated lens and death from rupture of dissecting aneurysm of aorta. JAMA 1943; 123: 88-9.

4. 4. Dietz HC, Cutting GR, Pyeritz RE, et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature 1991; 352: 337-9.

5. 5. De Paepe A, Devereux RB, Dietz HC, Hennekam RC, Pyeritz RE. Revised diagnostic criteria for the marfan syndrome. Am J Med Genet 1996; 62: 417-26.

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