نتایج جستجو برای: hereditary hemochromatosis

تعداد نتایج: 85981  

Journal: :The Journal of clinical investigation 2013
Ningning Zhao An-Sheng Zhang Caroline A Enns

Hepcidin is a key hormone that is involved in the control of iron homeostasis in the body. Physiologically, hepcidin is controlled by iron stores, inflammation, hypoxia, and erythropoiesis. The regulation of hepcidin expression by iron is a complex process that requires the coordination of multiple proteins, including hemojuvelin, bone morphogenetic protein 6 (BMP6), hereditary hemochromatosis ...

Journal: :Haematologica 2009
Marcel van Deuren Joyce J C Kroot Dorine W Swinkels

It is currently unknown if the increase of the hepatic iron regulatory hormone hepcidin during inflammation in man depends on an intact HFE-protein. Here we describe the temporal relationship of serum hepcidin, serum iron and cytokines in a patient with HFE-related (C282Y homozygous) hereditary hemochromatosis who was treated for an auto-inflammatory condition, i.e. variant Schnitzler's syndrom...

Journal: :American journal of physiology. Cell physiology 2008
Daniel F Wallace Lesa Summerville Emily M Crampton V Nathan Subramaniam

Transferrin receptor 2 (TfR2), a homologue of transferrin receptor 1 (TfR1), is a key molecule involved in the regulation of iron homeostasis. Mutations in TfR2 result in iron overload with similar features to HFE-associated hereditary hemochromatosis. The precise role of TfR2 in iron metabolism and the functional consequences of disease-causing mutations have not been fully determined. We have...

Journal: :Gastroenterology 1998
C E McLaren G J McLachlan J W Halliday S I Webb B A Leggett E C Jazwinska D H Crawford V R Gordeuk G D McLaren L W Powell

BACKGROUND & AIMS An elevated transferrin saturation is the earliest phenotypic abnormality in hereditary hemochromatosis. Determination of transferrin saturation remains the most useful noninvasive screening test for affected individuals, but there is debate as to the appropriate screening level. The aims of this study were to estimate the mean transferrin saturation in hemochromatosis heteroz...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
L Salter-Cid A Brunmark Y Li D Leturcq P A Peterson M R Jackson Y Yang

Hereditary hemochromatosis is a common autosomal recessive disorder of iron metabolism. Recent demonstration of an association between transferrin receptor (TfR) and HFE, a major histocompatibility complex class I-like molecule that has been implicated to play a role in hereditary hemochromatosis, further strengthens the notion that HFE is involved in iron metabolism. Herein we show that TfR is...

2011
Ashraf Haddad Gopal C. Kowdley Timothy M. Pawlik Steven C. Cunningham

Hereditary etiologies of pancreatic and hepatobiliary cancers are increasingly recognized. An estimated >10% of pancreatic and increasing number of hepatobiliary cancers are hereditary. The cumulative risk of hereditary pancreatic cancer ranges from measurable but negligible in cystic fibrosis to a sobering 70% in cases of hereditary pancreatitis. Candidates for pancreatic cancer surveillance a...

Journal: :Clinical Orthopaedics & Related Research 2011

2016
Nina Wrobel Torben Pottgiesser Philipp Birkner Peter Deibert Christoph Ahlgrim

INTRODUCTION Hereditary hemochromatosis features a dysregulated iron absorption leading to iron overload and organ damage. The regulation of total hemoglobin mass during depletion of iron deposits by therapeutic phlebotomy has not been studied. CASE PRESENTATION The initial ferritin level of the 52-year-old male subject was 1,276 μg/l. Despite successful depletion of iron stores (ferritin<Sub...

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