Hereditary Haemochromatosis (HH)
- What is Hereditary Haemochromatosis?
- Statistics on Hereditary Haemochromatosis
- Risk Factors for Hereditary Haemochromatosis
- Progression of Hereditary Haemochromatosis
- How is Hereditary Haemochromatosis Diagnosed?
- Prognosis of Hereditary Haemochromatosis
- How is Hereditary Haemochromatosis Treated?
- Hereditary Haemochromatosis References
What is Hereditary Haemochromatosis?
Hereditary Haemochromatosis is an inherited disorder of iron metabolism where there is increased intestinal iron absorption leading to deposition and subsequent damage in multiple organs (joints, liver, heart, pancreas and pituitary).HH is an autosomal recessive condition - hence a person needs both copies (one from each parent) of the affectred gene to be abnormal to develop the disease.
Statistics on Hereditary Haemochromatosis
Hereditary Haemochromatosis is a common disease. Approximately 1 in 10 individuals carry one abnormal copy of the affected gene (carriers, heterozygotes) and about 1 in 400 have both copies of the abnormal gene.Middle aged males are more frequently and severely affected than women. The disease tends to present approximately ten years later in women (menstrual blood loss is protective).
Risk Factors for Hereditary Haemochromatosis
As mentioned above, having two copies of the abnormal (HFE) gene is the most important causative factor. Other factors such as excess alcohol consumption or dietary iron excess may also play a part.Haemochromatosis may also occur as a secondary event - that is not as a result of the genetic factors. It may occur with some serious anaemias (e.g. thalassaemia major) with repeated blood transfusions, due to dietery iron excess (rarely in western society) and also with chronic liver disease.
Progression of Hereditary Haemochromatosis
The course of the disease depends on a number of factors including sex, dietary iron intake, presence of associated liver toxins (especially alcohol) and genetics.With progressive iron accumulation and fibrosis, the following complications may be seen:
How is Hereditary Haemochromatosis Diagnosed?
Prognosis of Hereditary Haemochromatosis
The prognosis largely depends on whether the disease is diagnosed early and treatment started accordingly - when there is normal life expectancy. If the disease is diagnosed later, after the onset of liver cirrhosis, diabetes, and heart abnormalities - then these are irreversible and life expectancy is shortened. Gonadal failure is also irreversive, hence impotence will not reverse with treatment of the disease.
How is Hereditary Haemochromatosis Treated?
Treatment for the disease is venesection (the taking of blood). This should be performed initially one to two times weekly until there is a moderate iron deficiency. Because iron will continue to accumulate venesection is needed every 2-3 months (1 unit) for the rest of the individual's life.Screening:1st degree relatives should be tested for an overload of iron and for the abnormal gene.
Hereditary Haemochromatosis References
- Braunwald, Fauci, Kasper, Hauser, Longo, Jameson. Harrison's Principles of Internal Medicine. 15th Edition. McGraw-Hill. 2001
- Cotran, Kumar, Collins 6th edition. Robbins Pathologic Basis of Disease. WB Saunders Company. 1999.
- Haslet C, Chiliers ER, Boon NA, Colledge NR. Principles and Practice of Medicine. Churchill Livingstone 2002.
- Hurst JW (Editor-in-chief). Medicine for the practicing physician. 4th edition Appleton and Lange 1996.
- Kumar P, Clark M. CLINICAL MEDICINE. WB Saunders 2002
- Longmore M, Wilkinson I, Torok E. OXFORD HANDBOOK OF CLINICAL MEDICINE. Oxford Universtiy Press. 2001
- McLatchie G and LEaper DJ (editors). Oxford Handbook of Clinical Surgery 2nd Edition. Oxford University Press 2002.
- MEDLINE Plus
- Raftery AT Churchill's pocketbook of Surgery. Churchill Livingsone 2001.
- Tjandra, JJ, Clunie GJ, Thomas, RJS,; Textbook of Surgery, 2nd Ed, Blackwell Science, Asia. 2001.
|Modified: 7/2/2008||Created: 13/9/2003|
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