Hemochromatosis Research Paper

Introduction: Hemochromatosis is a disorder which involves to much iron overload in the body, in some cases can be fatal. Hemochromatosis is inherited if each parent has that mutation. Hemochromatosis can develop from your everyday diet. It has a autosomal recessive pattern. To help raise money for the awareness you can help the foundation supporting the disorder, called Americanhs.org.

Symptoms
Some people with hemochromatosis complain of these symptoms, but not all are specific indicators of hemochromatosis. The symptoms are lack of energy, abdominal pain, memory fog, heart flutters and some have a irregular heartbeat. Some of these diseases can develop if hemochromatosis is left untreated, osteoporosis, osteoarthritis, cirrhosis,
You inherit one gene called HFE gene from each of your parents. The HFE gene has two common mutations, C282Y and H63D. Genetic testing can reveal whether you have these mutations in your gene. Hemochromatosis is found on chromosome 6.

Treatments and therapies
Therapeutic phlebotomy, iron chelation therapy and dietary changes can all help with hemochromatosis. The goals with treating hemochromatosis include, reducing the amount of iron in your body to normal levels, to prevent organ damage. Treating complications of the disease, maintaining a normal amount of iron in your body for the rest of your life. Dietary changes, Avoid taking iron including iron pills and multivitamins that contain iron. Limit alcohol intake, drinking alcohol increases the risk of liver disease.

Inheritance pattern
Types 1, 2 and 3 hemochromatosis are inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. Most often, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene but don't show signs and symptoms of the condition. Hemochromatosis is usually found equally in both genders, if there parents have that