20-year follow-up study of Danish HHT patients—survival and causes of death

BACKGROUND: Hereditary Haemorrhagic Telangiectasia (HHT) is a dominantly inheritable disorder, with a wide variety of clinical manifestations due to presence of multiple arteriovenous manifestations. The most common mutations are found in HHT1 (ENG) and HHT2 (ACVRL1) patients, causing alterations in...

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Detalles Bibliográficos
Autores principales: Kjeldsen, Anette, Aagaard, Katrine Saldern, Tørring, Pernille Mathiesen, Möller, Sören, Green, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120428/
https://www.ncbi.nlm.nih.gov/pubmed/27876060
http://dx.doi.org/10.1186/s13023-016-0533-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120428/
https://www.ncbi.nlm.nih.gov/pubmed/27876060
http://dx.doi.org/10.1186/s13023-016-0533-9

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