Previous studies have shown that hemochromatosis is an inherited, autosomal-recessive disease and that the gene is closely linked to the HLA locus on chromosome 6. We obtained a lod score for linkage of +9.8 for a recombination fraction of 0.0 and a gene frequency of 0.056, the frequency estimated in this population. We studied the phenotypic expression of the disease in 261 members of 10 pedigrees. In heterozygotes over 20 years of age, there was an intermediate increase in transferrin saturation and a limited increase in hepatic iron but no clinical manifestations. In male heterozygotes, the average amount of iron in the liver increased from about 0.2 to 1.3 g. Abnormal homozygotes accumulated iron progressively with time, with men accumulating about 18 g in the liver. All measurements of iron status were increased in abnormal homozygotes. Hemochromatosis is inherited as an autosomal-recessive disease, with partial biochemical expression in heterozygotes.
This article has been cited by other articles:
Chen, J., Enns, C. A.
(2007). The Cytoplasmic Domain of Transferrin Receptor 2 Dictates Its Stability and Response to Holo-transferrin in Hep3B Cells. J. Biol. Chem.
282: 6201-6209
[Abstract][Full Text]
Miranda, C. J., Makui, H., Soares, R. J., Bilodeau, M., Mui, J., Vali, H., Bertrand, R., Andrews, N. C., Santos, M. M.
(2003). Hfe deficiency increases susceptibility to cardiotoxicity and exacerbates changes in iron metabolism induced by doxorubicin. Blood
102: 2574-2580
[Abstract][Full Text]
Schwartz, K. A., Li, Z., Schwartz, D. E., Cooper, T. G., Braselton, W. E.
(2002). Earliest cardiac toxicity induced by iron overload selectively inhibits electrical conduction. J. Appl. Physiol.
93: 746-751
[Abstract][Full Text]
Li, C K, Chik, K W, Lam, C W K, To, K F, Yu, S C H, Lee, V, Shing, M M K, Cheung, A Y K, Yuen, P M P
(2002). Liver disease in transfusion dependent thalassaemia major. Arch. Dis. Child.
86: 344-347
[Abstract][Full Text]
Waheed, A., Grubb, J. H., Zhou, X. Y., Tomatsu, S., Fleming, R. E., Costaldi, M. E., Britton, R. S., Bacon, B. R., Sly, W. S.
(2002). Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis. Proc. Natl. Acad. Sci. USA
10.1073/pnas.042701499v1
[Abstract][Full Text]
Kushner, J. P., Porter, J. P., Olivieri, N. F.
(2001). Secondary Iron Overload. ASH Education Book
2001: 47-61
[Abstract][Full Text]
Bhavnani, M, Lloyd, D, Bhattacharyya, A, Marples, J, Elton, P, Worwood, M
(2000). Screening for genetic haemochromatosis in blood samples with raised alanine aminotransferase. Gut
46: 707-710
[Abstract][Full Text]
Pascoe, A, Kerlin, P, Steadman, C, Clouston, A, Jones, D, Powell, L, Jazwinska, E, Lynch, S, Strong, R
(1999). Spur cell anaemia and hepatic iron stores in patients with alcoholic liver disease undergoing orthotopic liver transplantation. Gut
45: 301-305
[Abstract][Full Text]
Olivieri, N. F.
(1999). The {beta}-Thalassemias. NEJM
341: 99-109
[Full Text]
Fleming, R. E., Migas, M. C., Zhou, X., Jiang, J., Britton, R. S., Brunt, E. M., Tomatsu, S., Waheed, A., Bacon, B. R., Sly, W. S.
(1999). Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: Increased duodenal expression of the iron transporter DMT1. Proc. Natl. Acad. Sci. USA
96: 3143-3148
[Abstract][Full Text]
Waheed, A., Parkkila, S., Saarnio, J., Fleming, R. E., Zhou, X. Y., Tomatsu, S., Britton, R. S., Bacon, B. R., Sly, W. S.
(1999). Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum. Proc. Natl. Acad. Sci. USA
96: 1579-1584
[Abstract][Full Text]
Burt, M J, George, P M, Upton, J D, Collett, J A, Frampton, C M A, Chapman, T M, Walmsley, T A, Chapman, B A
(1998). The significance of haemochromatosis gene mutations in the general population: implications for screening. Gut
43: 830-836
[Abstract][Full Text]
George, D K, Ramm, G A, Powell, L W, Fletcher, L M, Walker, N I, Cowley, L L, Crawford, D H G
(1998). Evidence for altered hepatic matrix degradation in genetic haemochromatosis. Gut
42: 715-720
[Abstract][Full Text]
Zhou, X. Y., Tomatsu, S., Fleming, R. E., Parkkila, S., Waheed, A., Jiang, J., Fei, Y., Brunt, E. M., Ruddy, D. A., Prass, C. E., Schatzman, R. C., O'Neill, R., Britton, R. S., Bacon, B. R., Sly, W. S.
(1998). HFE gene knockout produces mouse model of hereditary hemochromatosis. Proc. Natl. Acad. Sci. USA
95: 2492-2497
[Abstract][Full Text]
Waheed, A., Parkkila, S., Zhou, X. Y., Tomatsu, S., Tsuchihashi, Z., Feder, J. N., Schatzman, R. C., Britton, R. S., Bacon, B. R., Sly, W. S.
(1997). Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with beta 2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proc. Natl. Acad. Sci. USA
94: 12384-12389
[Abstract][Full Text]
Parkkila, S., Waheed, A., Britton, R. S., Feder, J. N., Tsuchihashi, Z., Schatzman, R. C., Bacon, B. R., Sly, W. S.
(1997). Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract. Proc. Natl. Acad. Sci. USA
94: 2534-2539
[Abstract][Full Text]
Olivieri, N. F., Brittenham, G. M.
(1997). Iron-Chelating Therapy and the Treatment of Thalassemia. Blood
89: 739-761
[Full Text]
Bulaj, Z. J., Griffen, L. M., Jorde, L. B., Edwards, C. Q., Kushner, J. P.
(1996). Clinical and Biochemical Abnormalities in People Heterozygous for Hemochromatosis. NEJM
335: 1799-1805
[Abstract][Full Text]
Powell, L. W., Jazwinska, E. C.
(1996). Hemochromatosis in Heterozygotes. NEJM
335: 1837-1839
[Full Text]
McLaren, C. E
(1996). Mixture models in haematology: a series of case studies. Stat Methods Med Res
5: 129-153
[Abstract]
Ransohoff, D. F., Muir, W. A.
(1982). Diagnostic Workup Bias in the Evaluation of a Test: Serum Ferritin and Hereditary Hemochromatosis. Med Decis Making
2: 139-145
Waheed, A., Grubb, J. H., Zhou, X. Y., Tomatsu, S., Fleming, R. E., Costaldi, M. E., Britton, R. S., Bacon, B. R., Sly, W. S.
(2002). Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis. Proc. Natl. Acad. Sci. USA
99: 3117-3122
[Abstract][Full Text]