Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosis

HFE-related hereditary haemochromatosis (HH) is an iron overload disease attributed to the highly prevalent homozygosity for the C282Y mutation in the HFE gene. The pathophysiology of this error in iron metabolism is not completely elucidated yet, although deficiency of the iron regulatory hormone h...

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Veröffentlicht in:	Netherlands journal of medicine 2007-12, Vol.65 (11), p.419-424
Hauptverfasser:	JACOBS, E. M. G, VERBEEK, A. L. M, KREEFTENBERG, H. G, VAN DEURSEN, C. Th. B. M, MARX, J. J. M, STALENHOEF, A. F. H, SWINKELS, D. W, DE VRIES, R. A
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences General aspects Hemochromatosis - diagnosis Hemochromatosis - genetics Hemochromatosis Protein Histocompatibility Antigens Class I - genetics Humans Mass Screening Medical sciences Membrane Proteins - genetics Metabolic diseases Metals (hemochromatosis...) Mutation Other metabolic disorders Time Factors
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