Key-interventions derived from three evidence based guidelines for management and follow-up of patients with HFE haemochromatosis

BACKGROUND: HFE-related hereditary haemochromatosis (HH) is a common autosomal recessive disorder with clinical manifestations ranging from asymptomatic disease to possible life-threatening complications. Cirrhosis, hepatocellular carcinoma, diabetes mellitus or osteoporosis can develop in HH patien...

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Detalles Bibliográficos
Autores principales: Vanclooster, Annick, Wollersheim, Hub, Vanhaecht, Kris, Swinkels, Dorine, Aertgeerts, Bert, Cassiman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062877/
https://www.ncbi.nlm.nih.gov/pubmed/27733158
http://dx.doi.org/10.1186/s12913-016-1835-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062877/
https://www.ncbi.nlm.nih.gov/pubmed/27733158
http://dx.doi.org/10.1186/s12913-016-1835-2

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