Haemochromatosis type 3
Haemochromatosis type 3 is a rare genetic disorder characterized by the excessive accumulation of iron in the body. This condition is caused by mutations in the TFRC gene and is inherited in an autosomal recessive manner.
Symptoms[edit | edit source]
The symptoms of Haemochromatosis type 3 typically begin in adulthood and may include fatigue, arthritis, and liver disease. Some affected individuals may also develop heart disease, diabetes, impotence, and skin discoloration.
Causes[edit | edit source]
Haemochromatosis type 3 is caused by mutations in the TFRC gene. This gene provides instructions for making a protein that is involved in the transport of iron into cells. Mutations in the TFRC gene disrupt the normal regulation of iron balance in the body, leading to the accumulation of iron in various tissues and organs.
Diagnosis[edit | edit source]
The diagnosis of Haemochromatosis type 3 is based on the presence of characteristic symptoms, a detailed patient history, a thorough clinical evaluation, and a variety of specialized tests. These tests may include blood tests to measure iron levels, genetic testing to identify mutations in the TFRC gene, and imaging studies to assess the extent of iron accumulation in the body.
Treatment[edit | edit source]
The treatment of Haemochromatosis type 3 is aimed at reducing the amount of iron in the body to normal levels. This is typically achieved through a procedure called phlebotomy, in which blood is removed from the body on a regular basis. Other treatment options may include dietary changes to reduce iron intake and medications to help remove excess iron from the body.
Prognosis[edit | edit source]
The prognosis for individuals with Haemochromatosis type 3 varies depending on the severity of the condition and the response to treatment. With early diagnosis and appropriate treatment, most individuals with this condition can lead normal, healthy lives.
See also[edit | edit source]
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