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Valve-sparing aortic root replacement in Loeys-Dietz syndrome and a novel mutation in TGFBR2.

作者信息

Kasar Taner, Gezdirici Alper, Ayyıldız Pelin, Haydin Sertaç, Güzeltaş Alper

机构信息

Department of Pediatric Cardiology, İstanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital; İstanbul-Turkey.

出版信息

Anatol J Cardiol. 2018 Jan;19(1):74-77. doi: 10.14744/AnatolJCardiol.2017.7911.

DOI:10.14744/AnatolJCardiol.2017.7911
PMID:29339704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5864794/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/93241a96cd36/AJC-19-74-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/478d0c73f1b9/AJC-19-74-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/ffcfbec2b3e4/AJC-19-74-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/93241a96cd36/AJC-19-74-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/478d0c73f1b9/AJC-19-74-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/ffcfbec2b3e4/AJC-19-74-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eff/5864794/93241a96cd36/AJC-19-74-g003.jpg

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引用本文的文献

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Bicuspid Aortic Valve: An Update in Morphology, Genetics, Biomarker, Complications, Imaging Diagnosis and Treatment.二叶式主动脉瓣:形态学、遗传学、生物标志物、并发症、影像诊断及治疗的最新进展
Front Physiol. 2019 Jan 30;9:1921. doi: 10.3389/fphys.2018.01921. eCollection 2018.

本文引用的文献

1
Aortic Root Replacement for Children With Loeys-Dietz Syndrome.洛伊斯-迪茨综合征患儿的主动脉根部置换术。
Ann Thorac Surg. 2017 May;103(5):1513-1518. doi: 10.1016/j.athoracsur.2017.01.053. Epub 2017 Mar 31.
2
Cardiovascular operations for Loeys-Dietz syndrome: Intermediate-term results.洛伊茨-迪茨综合征的心血管手术:中期结果。
J Thorac Cardiovasc Surg. 2017 Feb;153(2):406-412. doi: 10.1016/j.jtcvs.2016.10.088. Epub 2016 Nov 16.
3
Loeys-Dietz syndrome: a primer for diagnosis and management.洛伊迪茨综合征:诊断与管理入门
Genet Med. 2014 Aug;16(8):576-87. doi: 10.1038/gim.2014.11. Epub 2014 Feb 27.
4
Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2.与TGFB2基因突变相关的胸主动脉瘤和夹层合并严重二尖瓣疾病。
Int J Cardiol. 2013 May 25;165(3):584-7. doi: 10.1016/j.ijcard.2012.09.029. Epub 2012 Oct 25.
5
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis.SMAD3 基因突变可导致综合征型主动脉瘤和夹层,伴发病症有早发性骨关节炎。
Nat Genet. 2011 Feb;43(2):121-6. doi: 10.1038/ng.744. Epub 2011 Jan 9.
6
Aneurysm syndromes caused by mutations in the TGF-beta receptor.由转化生长因子-β受体突变引起的动脉瘤综合征
N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695.