Executive summary of the 12th HHT international scientific conference

被引：0

作者：

Jillian W. Andrejecsk

Anna E. Hosman

Luisa M. Botella

Claire L. Shovlin

Helen M. Arthur

Sophie Dupuis-Girod

Elisabetta Buscarini

Christopher C. W. Hughes

Franck Lebrin

Christine L. Mummery

Marco C. Post

Johannes J. Mager

机构：

[1] University of California Irvine,Department of Molecular Biology and Biochemistry

[2] St. Antonius Hospital,Department of Pulmonology

[3] Centro de Investigaciones Biológicas,Vascular Science, National Heart and Lung Institute

[4] Consejo Superior de Investigaciones Científicas (CSIC),Institute of Genetic Medicine, Centre for Life

[5] and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER),Gastroenterology and Endoscopy Department, Reference Center for Hereditary Hemorrhagic Telangiectasia

[6] Imperial College London,Einthoven Laboratory for Experimental Vascular Medicine, Department of Internal Medicine (Nephrology)

[7] Newcastle University,Department of Anatomy and Embryology

[8] Hospices Civils de Lyon,Department of Cardiology

[9] Genetic Unit and HHT Reference Center,undefined

[10] Bron,undefined

[11] School of Medical and University Lyon 1,undefined

[12] Maggiore Hospital,undefined

[13] ASST Crema,undefined

[14] Leiden University Medical Center,undefined

[15] CNRS UMR 7587,undefined

[16] INSERM U979,undefined

[17] Institut Langevin,undefined

[18] ESPCI,undefined

[19] Leiden University Medical Center,undefined

[20] St. Antonius Hospital,undefined

来源：

Angiogenesis | 2018年 / 21卷

关键词：

HHT; Hereditary hemorrhagic telangiectasia; Endoglin; Activin receptor-like kinase 1 (ALK1); Arteriovenous malformation; Epistaxis;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Hereditary hemorrhagic telangiectasia is an autosomal dominant trait affecting approximately 1 in 5000 people. A pathogenic DNA sequence variant in the ENG, ACVRL1 or SMAD4 genes, can be found in the majority of patients. The 12th International Scientific HHT Conference was held on June 8–11, 2017 in Dubrovnik, Croatia to present and discuss the latest scientific achievements, and was attended by over 200 scientific and clinical researchers. In total 174 abstracts were accepted of which 58 were selected for oral presentations. This article covers the basic science and clinical talks, and discussions from three theme-based workshops. We focus on significant emergent themes and unanswered questions. Understanding these topics and answering these questions will help to define the future of HHT research and therapeutics, and ultimately bring us closer to a cure.

引用

页码：169 / 181

页数：12

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