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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Int Med Res
Egile Nagusiak: Major, Tamás, Csobay-Novák, Csaba, Gindele, Réka, Szabó, Zsuzsanna, Bora, László, Jóni, Natália, Rácz, Tamás, Karosi, Tamás, Bereczky, Zsuzsanna
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: SAGE Publications 2019
Gaiak:
Special Issue: Hematology
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7607172/
https://ncbi.nlm.nih.gov/pubmed/31510822
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060519860971
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