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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
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Genetic haemochromatosis: diagnosis and treatment of an iron overload disorder

Martin Johnson1, Gerri Mortimore2

  • 1School of Health and Society Nursing, University of Salford, Salford, England.

Nursing Standard (Royal College of Nursing (Great Britain) : 1987)
|September 20, 2022
PubMed

Genetic haemochromatosis is a potentially serious iron overload disorder, yet there is a lack of awareness of the condition among the public and many healthcare professionals. In the UK, around one in 150 people have the genetic mutations that cause the condition, meaning that they are at increased risk of developing iron overload. If undiagnosed, prolonged iron overload can lead to liver, heart and endocrine failure and may be fatal; however, early diagnosis, treatment and maintenance can enable patients to have a normal lifespan. This article provides an overview of genetic haemochromatosis, including its types, origins, signs and symptoms, diagnosis, screening and treatment.

Keywords:
bloodblood disorderscancerclinicalethical issuesgenetic disordersgenetic testinggeneticsprofessional

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