Diagnosis and treatment of genetic haemochromatosis

Milman, N.T.

Ugeskrift for Laeger 175(16): 1109-1112

2013


ISSN/ISBN: 1603-6824
PMID: 23651749
Document Number: 669824
Genetic haemochromatosis is a complex disorder/disease, which can be caused by a multiplicity of mutations in genes involved in iron metabolism being located on different chromosomes. In Caucasians, mutations in the HFE-gene account for the most common form of haemochromatosis (type 1). Non-HFE-haemochromatoses are less frequent and consist of juvenile haemochromatosis (type 2A and 2B) and TRF2-related haemochromatosis (type 3), which all respond to phlebotomies. The others comprise ferroportin disease (type 4A) atypical ferroportin disease (type 4B), acoeruloplasminaemia, atransferrinaemia and DMT1-associated haemochromatosis.

Document emailed within 1 workday
Secure & encrypted payments