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Severe Recurrent Epistaxis - The Main Symptom of Hereditary Haemorrhagic Teleangiectasia Cover

Severe Recurrent Epistaxis - The Main Symptom of Hereditary Haemorrhagic Teleangiectasia

Acta Medica Martiniana
Volume 18 (2018): Issue 3 (December 2018)
By: M Lucanska,  A Hajtman and  R Pecova  
Open Access
|Feb 2019

Authors

M Lucanska

miroslava.zarska@gmail.com

Clinic of Otorhinolaryngology and Head and Neck Surgery, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava and Martin University Hospital, Martin

A Hajtman

Clinic of Otorhinolaryngology and Head and Neck Surgery, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava and Martin University Hospital, Martin

R Pecova

Department of Pathological Physiology and Biomedical Centre, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin
DOI: https://doi.org/10.2478/acm-2018-0016 | Journal eISSN: 1338-4139 | Journal ISSN: 1335-8421
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Language: English
Page range: 42 - 48
Submitted on: Dec 4, 2018
|
Accepted on: Dec 20, 2018
|
Published on: Feb 23, 2019
Published by: Sciendo
In partnership with: Paradigm Publishing Services
Publication frequency: 3 issues per year
Keywords:
Hereditary haemorrhagic teleangiectasia,
Rendu-Osler-Weber syndrome,
epistaxis
Related subjects:
Medicine,
Clinical medicine,
Internal medicine,
Cardiology

© 2019 M Lucanska, A Hajtman, R Pecova, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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