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HaemochromatosisHaemochromatosis is a disorder of iron regulation (metabolism) in your body. It is a genetic condition that causes people to absorb excessive amounts of dietary iron. Because the regulation of iron absorption is "out of kilter", excess iron is stored in the tissue. The Irish Haemochromatosis Association is a support group for haemochromatosis patients and their families. In people without haemochromatosis the body only absorbs as much iron as it needs, with the rest being excreted by the body. Other problems that can be caused by excessive iron include heart disease, diabetes and arthritis. Haemochromatosis is an inherited (genetic) condition and is considered to be the most common genetic disease in the world. In New Zealand approximately one person in every 200 has the condition, while approximately one in seven are carriers. Both sexes are at risk, but women tend to develop the condition later in life, since regular menstrual periods deplete the body of iron. Haemochromatosis tends to be under-diagnosed, partly because its symptoms are similar to those caused by a range of other illnesses. Haemochromatosis is one of the most common hereditary diseases. Its main role is in making red blood cells, which carry oxygen to all parts of the body. When too much iron is taken up it slowly builds up in various parts of the body, including the liver, heart and pancreas. It may be many years before there are any symptoms of haemochromatosis and when problems do arise they are often very vague and can be confused with many other conditions. This is the most common of all the genetic conditions; it is even more common than cystic fibrosis or muscular dystrophy. Sometimes the skin has a ‘sun-tanned' colour. If the pancreas is affected, diabetic complications may occur. Heart problems such as palpitations and shortness of breath can also happen. Symptoms of HaemochromatosisSome Symptoms of Haemochromatosis :
Treatment of Haemochromatosis
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