Learning to live with hereditary haemochromatosis: a qualitative descriptive study

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15 صفحه اول

Hereditary haemochromatosis.

Haemochromatosis should currently refer to hereditary iron overload disorders presenting with a definite and common phenotype characterised by normal erythropoiesis, increased transferrin saturation and ferritin and primarily parenchymal iron deposition related to innate low (but normally regulated) production of the hepatic peptide hormone hepcidin. Since the discovery of the haemochromatosis ...

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Hereditary haemochromatosis

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Screening for hereditary haemochromatosis.

Hereditary haemochromatosis (HH) is a common autosomal recessive disorder of iron overload in Caucasian populations. Clinical manifestations usually occur in individuals homozygous for the C282Y mutation in the HFE gene product and who have developed significant iron loading. Current screening methods can detect affected individuals either prior to or early during disease evolution, enabling ea...

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ژورنال

عنوان ژورنال: Journal of Nursing and Healthcare of Chronic Illness

سال: 2011

ISSN: 1752-9816

DOI: 10.1111/j.1752-9824.2011.01086.x