Literature DB >> 22687666

An unusual cause for recurrent transient ischaemic attacks.

Baki Ejupi1, Shafick Gareeboo.   

Abstract

A 37-year-old gentleman with a known diagnosis of hereditary haemorrhagic telangiectasia was referred to the Chest Clinic with recurrent shortness of breath and transient ischaemic attacks. Following extensive investigations, his CT pulmonary angiogram showed arteriovenous malformation, which led to definitive treatment and complete withdrawal of symptoms.

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Year:  2011        PMID: 22687666      PMCID: PMC4545035          DOI: 10.1136/bcr.04.2011.4122

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  3 in total

1.  Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia.

Authors:  C L Shovlin; J E Jackson; K B Bamford; I H Jenkins; A R Benjamin; H Ramadan; E Kulinskaya
Journal:  Thorax       Date:  2007-11-02       Impact factor: 9.139

2.  Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia.

Authors:  Vincent Cottin; Henri Plauchu; Jean-Yves Bayle; Martine Barthelet; Didier Revel; Jean-François Cordier
Journal:  Am J Respir Crit Care Med       Date:  2004-01-23       Impact factor: 21.405

Review 3.  Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.

Authors:  M E Begbie; G M F Wallace; C L Shovlin
Journal:  Postgrad Med J       Date:  2003-01       Impact factor: 2.401

  3 in total

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