Fatal rupture of pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasis and severe PAH

29-yr-old patient with hereditary haemorrhagic telangiectasia was referred to the present authors’ centre with progressive exertional dyspnoea. Pulmonary arterial hypertension (PAH) was suspected on Doppler echocardiography and confirmed by right heart catheterisation demonstrating severe PAH. Genet...

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Autors principals:	D. Montani, L. C. Price, B. Girerd, T. Chinet, P. Lacombe, G. Simonneau, M. Humbert
Format:	Artigo
Idioma:	Inglês
Publicat:	European Respiratory Society 2009-03-01
Col·lecció:	European Respiratory Review
Matèries:	Activin receptor-like kinase-1 arteriovenous malformation embolisation hereditary haemorrhagic telangiectasia pulmonary arterial hypertension rupture
Accés en línia:	http://err.ersjournals.com/cgi/content/full/18/111/42
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