Comorbidity among HHT patients and their controls in a 20 years follow-up period

BACKGROUND: Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant genetic disorder with a wide variety of clinical manifestations due to the presence of multiple arteriovenous malformations in various tissues and organs. OBJECTIVE: To study the need for hospital admittance in a group...

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Detalles Bibliográficos
Autores principales: Aagaard, Katrine Saldern, Kjeldsen, Anette Drøhse, Tørring, Pernille Mathiesen, Green, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295040/
https://www.ncbi.nlm.nih.gov/pubmed/30547819
http://dx.doi.org/10.1186/s13023-018-0962-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295040/
https://www.ncbi.nlm.nih.gov/pubmed/30547819
http://dx.doi.org/10.1186/s13023-018-0962-8

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