Robert S. Bonser, Domenico Pagano, Axel Haverich, Jorge's Controversies in Aortic Dissection and Aneurysmal Disease PDF

By Robert S. Bonser, Domenico Pagano, Axel Haverich, Jorge Mascaro

ISBN-10: 1447156218

ISBN-13: 9781447156215

ISBN-10: 1447156226

ISBN-13: 9781447156222

In this e-book the authors assessment the surgical administration of sufferers with aortic ailment. This frequently debatable region of administration finds many recommendations open to cardiovascular expert. This reference stories each one controversy and offers useful solutions to the cardiac physician and may support them display the spectrum of issues and their management.

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Hum Mutat. 2007;28:387–95. 44. Hucthagowder V, Sausgruber N, Kim KH, Angle B, Marmorstein LY, Urban Z. Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. Am J Hum Genet. 2006;78:1075–80. 45. Loeys B, Van Maldergem L, Mortier G, et al. Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa. Hum Mol Genet. 2002;11:2113–8. 46. Dasouki M, Markova D, Garola R, et al. Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa.

6 years; median survival: 48 years. 7 years. 3 %). Fatal complications during or immediately after vascular surgery occur in 45 %. 55). 50 % of females with 45, X die before age of ~62 years. The estimated incidence of AOD is 36 per 100,000 Turner’s syndrome years, compared with an incidence of 6 per 100,000 in the general population. The incidence of AOD is also reported as ~618 cases per 100,000 TS-years (almost 100-fold higher than for women in general. Onset of AOD between age 20–40 years. Two-thirds AOD-A; on-third AOD-B.

Le Goff C, Mahaut C, Wang LW, et al. Mutations in the TGFbeta binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias. Am J Hum Genet. 2011;89:7–14. Le Goff C, Morice-Picard F, Dagoneau N, et al. ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGFbeta bioavailability regulation. Nat Genet. 2008;40:1119–23. Loeys BL, Gerber EE, Riegert-Johnson D, et al. Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.

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Controversies in Aortic Dissection and Aneurysmal Disease by Robert S. Bonser, Domenico Pagano, Axel Haverich, Jorge Mascaro

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