Zoeken
Hemochromatosis
/hˌiːməkɹˌəʊmɐtˈəʊsɪs/
/hˌiːməkɹˌoʊmɐtˈoʊsɪs/Hemochromatosis
01
hemochromatose
a genetic disorder characterized by excessive absorption and accumulation of iron in the body, leading to potential organ damage
What is "hemochromatosis"?
Hemochromatosis is a genetic disorder that causes the body to absorb too much iron from the diet, leading to an excess buildup of iron in various organs and tissues. It is typically characterized by symptoms such as fatigue, joint pain, abdominal pain, and skin discoloration. Over time, untreated hemochromatosis can lead to serious complications such as liver damage, diabetes, heart problems, and arthritis. Treatment for hemochromatosis usually involves regular removal of blood to reduce iron levels in the body.
hemochromatosis
n
Voorbeeld
Hemochromatosis diagnosis involves blood and genetic tests.
Hemochromatosis is primarily caused by mutations in the HFE gene.
Symptoms of hemochromatosis may include fatigue, joint pain, and abdominal discomfort.
Genetic counseling is recommended for family members of individuals with hemochromatosis.
Early detection and intervention are crucial to prevent complications associated with hemochromatosis.
