Hemochromatosis due to the HFE mutation C282Y causes a progressive iron overload. The mortality occurs after 50 years. Repeated bleeding is an effective treatment with marginal side effects. The rationale for screening, debated for 60 years, depends on the penetrance and the effectiveness of treatment relatively to economic and social issues. This work provides evidence from cohort LOGIFER, 25 years old at the CHU of Rennes, composed of 1835 homozygous: consultants from CHU, from targeted surveys, referred to the NRC or related. The reasons for recruitment, gender and age have changed. 2/3 of patients are probants, half of them coming from screening, providing better representativity. The sex ratio was 1.2. They are characterized by skin pi...
L'hémochromatose génétique liée au gène HFE (HG) se caractérise par une augmentation de la saturatio...
Background: Most persons who are homozygous for C282Y, the HFE allele most commonly asssociated with...
Introduction: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
Hemochromatosis due to the HFE mutation C282Y causes a progressive iron overload. The mortality occu...
L'hémochromatose HFE due à la mutation C282Y entraine une surcharge en fer progressive. La surmortal...
HFE hemochromatosis is a disorder of iron metabolism related to the HFE gene whose mainmutation is C...
International audienceBackground & aims - Mortality studies in patients with hemochromatosis give co...
Depuis dix ans l'identification de la mutation C282Y a bouleversé la stratégie diagnostique de l'hém...
© 2018 Sim Yee OngHFE haemochromatosis is the most common iron overload disease. Since the discovery...
Background: Most persons who are homozygous for C282Y, the HFE allele most commonly asssociated with...
Iron overload (hemochromatosis) can cause serious, symptomatic disease that is preventable if detect...
L’hémochromatose HFE est une maladie du métabolisme du fer liée au gène HFE dont la principale mutat...
International audienceA number of human disorders are related to chronic iron overload, either of ge...
L hémochromatose héréditaire se caractérise par une hyperabsorption du fer conduisant à une accumula...
A doença hepática associada a sobrecarga de ferro pode ocorrer devido a causas genéticas ou secundár...
L'hémochromatose génétique liée au gène HFE (HG) se caractérise par une augmentation de la saturatio...
Background: Most persons who are homozygous for C282Y, the HFE allele most commonly asssociated with...
Introduction: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...
Hemochromatosis due to the HFE mutation C282Y causes a progressive iron overload. The mortality occu...
L'hémochromatose HFE due à la mutation C282Y entraine une surcharge en fer progressive. La surmortal...
HFE hemochromatosis is a disorder of iron metabolism related to the HFE gene whose mainmutation is C...
International audienceBackground & aims - Mortality studies in patients with hemochromatosis give co...
Depuis dix ans l'identification de la mutation C282Y a bouleversé la stratégie diagnostique de l'hém...
© 2018 Sim Yee OngHFE haemochromatosis is the most common iron overload disease. Since the discovery...
Background: Most persons who are homozygous for C282Y, the HFE allele most commonly asssociated with...
Iron overload (hemochromatosis) can cause serious, symptomatic disease that is preventable if detect...
L’hémochromatose HFE est une maladie du métabolisme du fer liée au gène HFE dont la principale mutat...
International audienceA number of human disorders are related to chronic iron overload, either of ge...
L hémochromatose héréditaire se caractérise par une hyperabsorption du fer conduisant à une accumula...
A doença hepática associada a sobrecarga de ferro pode ocorrer devido a causas genéticas ou secundár...
L'hémochromatose génétique liée au gène HFE (HG) se caractérise par une augmentation de la saturatio...
Background: Most persons who are homozygous for C282Y, the HFE allele most commonly asssociated with...
Introduction: HFE p.C282Y homozygosity is the most common cause of hereditary haemochromatosis. Ther...