Sunday 21 October 2012

Hereditary Hemochromatosis

Hereditary Hemochromatosis

In medicine, iron overload indicates accumulation of iron in the body from any cause. The most important causes are hereditary haemochromatosis (HHC), a genetic disorder, and transfusional iron overload, which can result from repeated blood transfusion. Organs commonly affected by haemochromatosis are the liver, heart, and endocrine glands. The causes can be distinguished between primary cases (hereditary or genetically determined) and less frequent secondary cases (acquired during life).[18] People of Celtic (Irish, Scottish, Welsh, Cornish, Breton etc.) origin have a particularly high incidence of whom about 10% are carriers of the gene and 1% sufferers from the condition. Routine treatment in an otherwise-healthy person consists of regularly scheduled phlebotomies (bloodletting). When first diagnosed, the phlebotomies may be fairly frequent, perhaps as often as once a week, until iron levels can be brought to within normal range. Once iron and other markers are within the normal range, phlebotomies may be scheduled every other month or every three months depending upon the patient's rate of iron loading. For those unable to tolerate routine blood draws, there is a chelating agent available for use. The drug Deferoxamine binds with iron in the bloodstream and enhances its elimination via urine and faeces. Typical treatment for chronic iron overload requires subcutaneous injection over a period of 8–12 hours daily. Two newer iron chelating drugs that are licensed for use in patients receiving regular blood transfusions to treat thalassaemia (and, thus, who develop iron overload as a result) are deferasirox and deferiprone.

Hereditary Hemochromatosis

Hereditary Hemochromatosis

Hereditary Hemochromatosis

Hereditary Hemochromatosis

Hereditary Hemochromatosis

Hereditary Hemochromatosis

Hereditary Hemochromatosis


Hereditary Hemochromatosis

Hereditary Hemochromatosis




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