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本文引用的文献

1
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.TGFB2 突变导致家族性胸主动脉瘤和夹层,伴有马凡综合征的轻微全身特征。
Nat Genet. 2012 Jul 8;44(8):916-21. doi: 10.1038/ng.2348.
2
A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome.SMAD4 肿瘤抑制基因的突变受到限制,这是 Myhre 综合征的基础。
Am J Hum Genet. 2012 Jan 13;90(1):161-9. doi: 10.1016/j.ajhg.2011.12.011.
3
Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.SMAD4 的 Mad 同源结构域 2 区的单个密码子突变导致 Myhre 综合征。
Nat Genet. 2011 Dec 11;44(1):85-8. doi: 10.1038/ng.1016.
4
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.外显子组测序鉴定出 SMAD3 突变是家族性胸主动脉瘤和夹层伴颅内及其他动脉动脉瘤的病因。
Circ Res. 2011 Sep 2;109(6):680-6. doi: 10.1161/CIRCRESAHA.111.248161. Epub 2011 Jul 21.
5
SMAD4 mutation segregating in a family with juvenile polyposis, aortopathy, and mitral valve dysfunction.SMAD4 突变在一个具有幼年性息肉病、主动脉病和二尖瓣功能障碍的家族中分离。
Am J Med Genet A. 2011 May;155A(5):1165-9. doi: 10.1002/ajmg.a.33968. Epub 2011 Apr 4.
6
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.
7
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.遗传性出血性毛细血管扩张症:病理生理学、诊断与治疗。
Blood Rev. 2010 Nov;24(6):203-19. doi: 10.1016/j.blre.2010.07.001. Epub 2010 Sep 25.
8
Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β.肥厚型心肌病小鼠的心脏纤维化是由非心肌细胞增殖介导的,需要 TGF-β。
J Clin Invest. 2010 Oct;120(10):3520-9. doi: 10.1172/JCI42028. Epub 2010 Sep 1.
9
SMAD4 mutation and the combined syndrome of juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia.SMAD4 突变与青少年息肉综合征和遗传性出血性毛细血管扩张症的联合综合征。
Thorax. 2010 Aug;65(8):745-6. doi: 10.1136/thx.2009.129932.
10
The revised Ghent nosology for the Marfan syndrome.修订版马凡综合征根特分类法。
J Med Genet. 2010 Jul;47(7):476-85. doi: 10.1136/jmg.2009.072785.

两名青少年息肉病综合征合并 SMAD4 基因突变患者的胸主动脉疾病。

Thoracic aortic disease in two patients with juvenile polyposis syndrome and SMAD4 mutations.

机构信息

MassGeneral Hospital for Children, Boston, MA, USA.

出版信息

Am J Med Genet A. 2013 Jan;161A(1):185-91. doi: 10.1002/ajmg.a.35659. Epub 2012 Dec 13.

DOI:10.1002/ajmg.a.35659
PMID:23239472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3535513/
Abstract

Dilation or aneurysm of the ascending aorta can progress to acute aortic dissection (Thoracic Aortic Aneurysms and Aortic Dissections, TAAD). Mutations in genes encoding TGF-β-related proteins (TGFBR1, TGFBR2, FBN1, and SMAD3) cause syndromic and inherited TAAD. SMAD4 mutations are associated with juvenile polyposis syndrome (JPS) and a combined JPS-hereditary hemorrhagic telangiectasia (HHT) known as JPS-HHT. A family with JPS-HHT was reported to have aortic root dilation and mitral valve abnormalities. We report on two patients with JPS-HHT with SMAD4 mutations associated with thoracic aortic disease. The first patient, an 11-year-old boy without Marfan syndrome features, had JPS and an apparently de novo SMAD4 mutation (c.1340_1367dup28). Echocardiography showed mild dilation of the aortic annulus and aortic root, and mild dilation of the sinotubular junction and ascending aorta. Computed tomography confirmed aortic dilation and showed small pulmonary arteriovenous malformations (PAVM). The second patient, a 34-year-old woman with colonic polyposis, HHT, and features of Marfan syndrome, had a SMAD4 mutation (c.1245_1248delCAGA). Echocardiography showed mild aortic root dilation. She also had PAVM and hepatic focal nodular hyperplasia. Her family history was significant for polyposis, HHT, thoracic aortic aneurysm, and dissection and skeletal features of Marfan syndrome in her father. These two cases confirm the association of thoracic aortic disease with JPS-HHT resulting from SMAD4 mutations. We propose that the thoracic aorta should be screened in patients with SMAD4 mutations to prevent untimely death from dissection. This report also confirms that SMAD4 mutations predispose to TAAD.

摘要

升主动脉扩张或动脉瘤可进展为急性主动脉夹层(胸主动脉瘤和主动脉夹层,TAAD)。编码 TGF-β相关蛋白(TGFBR1、TGFBR2、FBN1 和 SMAD3)的基因突变导致综合征性和遗传性 TAAD。SMAD4 突变与青少年息肉病综合征(JPS)和一种称为 JPS-HHT 的 JPS-遗传性出血性毛细血管扩张症(HHT)相关。据报道,一个 JPS-HHT 家族存在主动脉根部扩张和二尖瓣异常。我们报告了两例具有 SMAD4 突变的 JPS-HHT 患者,这些突变与胸主动脉疾病相关。第一例患者为 11 岁男孩,无马凡综合征特征,患有 JPS 和明显的新发 SMAD4 突变(c.1340_1367dup28)。超声心动图显示主动脉瓣环和主动脉根部轻度扩张,窦管交界处和升主动脉轻度扩张。计算机断层扫描证实了主动脉扩张,并显示小的肺动静脉畸形(PAVM)。第二例患者为 34 岁女性,患有结肠息肉、HHT 和马凡综合征特征,存在 SMAD4 突变(c.1245_1248delCAGA)。超声心动图显示主动脉根部轻度扩张。她还患有 PAVM 和肝局灶性结节性增生。她的家族史中有息肉病、HHT、胸主动脉瘤和夹层以及她父亲的马凡综合征骨骼特征的病史。这两例病例证实了 SMAD4 突变导致的 JPS-HHT 与胸主动脉疾病相关。我们建议对 SMAD4 突变患者进行胸主动脉筛查,以防止因夹层而意外死亡。本报告还证实 SMAD4 突变易导致 TAAD。