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Haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in a Scandinavian perspective
Linköping University, Faculty of Health Sciences. Linköping University, Department of Biomedicine and Surgery, Division of clinical chemistry. Östergötlands Läns Landsting, Centre for Laboratory Medicine, Department of Clinical Chemistry.
2007 (English)In: Scandinavian Journal of Clinical and Laboratory Investigation, ISSN 0036-5513, E-ISSN 1502-7686, Vol. 67, no 1Article in journal (Refereed) Published
Abstract [en]

Haemoglobinopathies (mainly thalassaemia and sickle-cell anaemia syndromes) and glucose-6-phosphate dehydrogenase deficiency (G6PD) are globally among the most prevalent single-genomic diseases. About 3 % of the world's population are heterozygotic for β-thalassaemia and about 1-2 % for sickle-cell anaemia, and it is estimated that more than 400 million people are affected by G6PD deficiency worldwide. The disorders are most prevalent in the Mediterranean area, in Asia and Africa. The Scandinavian countries, among others, have seen a boom in immigration during the past 20 years, and therefore migration makes haemoglobinopathies as well as G6PD deficiency increasingly more important from a differential diagnostic perspective in most countries. The purpose of the present special issue of the Journal is to summarize current epidemiological data and elucidate trends and practices in the laboratory diagnosis of these disorders. © 2007 Taylor & Francis.

Place, publisher, year, edition, pages
2007. Vol. 67, no 1
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:liu:diva-39387DOI: 10.1080/00365510601046359Local ID: 48151OAI: oai:DiVA.org:liu-39387DiVA: diva2:260236
Available from: 2009-10-10 Created: 2009-10-10 Last updated: 2017-12-13

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Theodorsson, Elvar

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