Pitfalls of delaying the diagnosis of hereditary haemorrhagic telangiectasia

Hereditary haemorrhagic telangiectasia (HHT; Osler–Weber–Rendu disease) is an autosomal dominant vascular disease characterized by nosebleeds, mucocutaneous telangiectases, visceral arteriovenous malformations (AVM) and a first-degree relative with HHT. Diagnosis is definite if three or four criteri...

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Detalles Bibliográficos
Autores principales: Major, Tamás, Csobay-Novák, Csaba, Gindele, Réka, Szabó, Zsuzsanna, Bora, László, Jóni, Natália, Rácz, Tamás, Karosi, Tamás, Bereczky, Zsuzsanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Special Issue: Hematology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607172/
https://www.ncbi.nlm.nih.gov/pubmed/31510822
http://dx.doi.org/10.1177/0300060519860971

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607172/
https://www.ncbi.nlm.nih.gov/pubmed/31510822
http://dx.doi.org/10.1177/0300060519860971

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