Osler-Weber-Rendu syndrome

Osler-Weber-Rendu syndrome

Hereditary haemorrhagic telangiectasia (HHT) is an uncommon autosomal dominant disease that occurs on mucocutaneous surfaces (ie, nose, gastrointestinal tract and skin), lung, liver and brain. 1 The Curacao criteria was developed for the diagnosis of HHT that contains epistaxis, family history, tela...

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Veröffentlicht in:BMJ case reports 2013-10, Vol.2013, p.bcr2013201034
Hauptverfasser: Abangah, Ghobad, Rashidbeygi, Milad
Format: Artikel
Sprache:eng
Schlagworte:
Diagnosis, Differential
Endoscopy, Gastrointestinal - methods
Female
Hemorrhage
Humans
Images In
Middle Aged
Middle East
Physical Examination
Telangiectasia, Hereditary Hemorrhagic - diagnosis
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Beschreibung
Zusammenfassung:Hereditary haemorrhagic telangiectasia (HHT) is an uncommon autosomal dominant disease that occurs on mucocutaneous surfaces (ie, nose, gastrointestinal tract and skin), lung, liver and brain. 1 The Curacao criteria was developed for the diagnosis of HHT that contains epistaxis, family history, telangiectasias and visceral lesions. 2 We were showed key recommendations with comments according to the Olitsky study for treatment of patient with HHT 3 (Appendix).
ISSN:1757-790X
1757-790X
DOI:10.1136/bcr-2013-201034