Ferroportin Disease

Ferroportin Disease

Ferroportin disease is a genetic condition caused by a mutation of the HFE gene. This mutation is responsible for excessive iron absorption in the body. Symptoms of this condition may vary. First signs may include weakness, diabetes, and liver damage. Other symptoms include change in skin colour, heart conditions, muscle pains, and hypothyroidism. Ferroportin disease can also cause infertility and erectile dysfunction. Blood tests are done to determine the cause of concern. Ferroportin disease is characterized by increased levels of ferritin and transferrin, which are proteins that store and transfer iron in the blood.

Summary Reference

Treatment:

1. http://www.merck.com/mmpe/sec11/ch145/ch145b.html?qt=ferroportin%20disease&alt=sh

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