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QJM Advance Access originally published online on February 20, 2006
QJM 2006 99(3):195-196; doi:10.1093/qjmed/hcl017
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© The Author 2006. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Correspondence

Myocardial infarction in a patient with normal coronary arteries and hereditary haemorrhagic telangiectasia

The first 10% of the full text of this article appears below.

Sir,

We read with interest the excellent paper by Gallitelli et al. on emergencies in hereditary haemorrhagic telangiectasia (HHT).1 HHT (or Osler-Weber-Rendu disease) is an uncommon autosomal dominant vascular disorder, related to an endoglin or activin-receptor-like kinase 1 (ALK1) gene mutation, resulting in multiorgan vascular dysplasia.2 HHT can lead to several . . . [Full Text of this Article]

S. Talha, C. Brandt, G. Maamari and J.-M. Mossard

Department of Cardiology

P. Germain

Department of Radiology

E. Andres

Department of Internal Medicine University Hospital of Strasbourg

email: emmanuel.andres@chru-strasbourg.fr


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