A retrospective cohort study on European Reference Network for Rare Vascular Diseases 5 outcome measures for Hereditary Haemorrhagic Telangiectasia in Denmark

A retrospective cohort study on European Reference Network for Rare Vascular Diseases 5 outcome measures for Hereditary Haemorrhagic Telangiectasia in Denmark

Abstract Background Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by several clinical symptoms including epistaxis, arteriovenous malformations (AVM), and telangiectasia. In 2018, European Reference Network for Rare Vascular Diseases (VASCERN) recommend...

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Bibliographic Details
Main Authors: Troels Hvelplund, Bibi Lange, Susanne Djernes Bird, Malene Korsholm, Anette Drøhse Kjeldsen
Format: Article
Language:English
Published: BMC 2022-01-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Hereditary Haemorrhagic Telangiectasia
VASCERN
PAVM screening
Iron deficiency
Online Access:https://doi.org/10.1186/s13023-021-02160-1

Internet

https://doi.org/10.1186/s13023-021-02160-1

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