Symptoms can include tiredness, weight loss, skin color changes, and more. The main treatment for hereditary hemochromatosis is regular blood ... in the HFE, HJV, HAM, TFR2, or SLC40A1 gene.

Secondary hemochromatosis happens for other reasons, like when someone has too much iron in their diet or has a condition that requires a lot of blood transfusions. The HFE gene controls how much ...

Meticulous family and HLA association studies followed ultimately by cloning of the HFE gene have dramatically changed our understanding of the natural history and manifestations of HH.

New research has found that men who carry a common genetic variant are twice as likely to develop dementia in their lifetime compared to women.

or if needed a DNA blood test to check for the presence of a faulty HFE gene. A liver biopsy may be carried out to assess whether liver damage has occurred. If you have close family members diagnosed ...

which sense when iron levels are high within the blood. Loss-of-function mutations of the HFE gene lead to an autosomal recessive iron-overload disorder referred to as hereditary hemochromatosis (HH).

INTRODUCTION: Hereditary hemochromatosis has been linked with C282Y and H63D mutations of the HFE gene encoding human hemochromatosis ... comprised 1516 DNA samples obtained either from cord blood or ...