Results 21 to 30 of about 28,106 (200)
The Arthropathy of Hemochromatosis Without Hemochromatosis [PDF]
Arthritis & Rheumatism, 1973 AbstractA 65‐year‐old man and his 62‐year‐old sister presented with joint pains and were found to have chondrocalcinosis. Both had elevations of serum iron and an increased saturation of iron binding protein. Biopsies revealed hemosiderin deposits in the parenchymal cells of the liver of both patients and the lining cells of the synovium of one ...
D A, Gordon, H A, Little
openaire +2 more sources
, 2021 Prevalences of Hemochromatosis-associated HFE genotypes and hemochromatosis phenotypes in African and European ...
Ronald T. Acton +2 more
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Ferroportin disease: pathogenesis, diagnosis and treatment
Haematologica, 2017 Ferroportin Disease (FD) is an autosomal dominant hereditary iron loading disorder associated with heterozygote mutations of the ferroportin-1 (FPN) gene.
Antonello Pietrangelo
doaj +1 more source
Prognostic Factors and Survival in Patients with Hereditary Hemochromatosis and Cirrhosis
Canadian Journal of Gastroenterology, 2006 OBJECTIVES: The survival of treated, noncirrhotic patients with hereditary hemochromatosis is similar to that of the general population. Less is known about the outcome of cirrhotic hereditary hemochromatosis patients.
Melanie D Beaton, Paul C Adams
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Case Reports in Oncology, 2020 Primary hemochromatosis is an inherited disorder, and the homeostatic iron regulator (HFE) gene C282Y mutation is a common cause of hemochromatosis in Europe. We are reporting a case of a 56-year-old female known to have hemochromatosis with the HFE gene
Mustafa A. Al-Tikrity, Mohamed A. Yassin
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Complete heart block with ventricular tachycardia in a patient with hemochromatosis
Saudi Journal of Medicine and Medical Sciences, 2014 Hereditary hemochromatosis is an inherited condition of dysregulated iron absorption, and usually presents with clinical features of hepatic dysfunction. Cardiac involvement as the presenting manifestation of hereditary hemochromatosis is rare. We report
Sajeer Kalathingathodika +3 more
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Hereditary hemochromatosis associated with autoimmune hemolytic anemia; A case report [PDF]
Journal of Preventive Epidemiology, 2019 Hereditary hemochromatosis is a disease associated with highly iron overload. This disease caused by genetic mutations inherited through family. Autoimmune hemolytic anemia is also an important autoimmune disease in which red blood cells (RBC) are ...
Masih Falahatian +2 more
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Novel mutation in ferroponin1 is associated with autosomal dominant hemochromatosis
, 2002 Hemochromatosis is a common disorder characterized by excess iron absorption and accumulation of iron in tissues. Usually hemochromatosis is inherited in an autosomal recessive pattern and is caused by mutations in the HFE gene.
Stephenson, Peter +13 more
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In-silico Molecular Analysis of Mutated Sequences of HFE1, HFE2, TFR2 and SLC40A1 causing Hemochromatosis Disease [PDF]
International Journal Bioautomation, 2011 Hemochromatosis is a disorder in iron metabolism that is characterized by excess iron absorption. There are two forms of hemochromatosis: primary hemochromatosis is caused by a problem with your genes.
Bilal Hussain +4 more
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