| Literature DB >> 17077770 |
Ahmed D Khattab1, Barry Rawlings, Ibtisam S Ali.
Abstract
Haemoglobinopathies refer to a range of genetically inherited disorders of red blood cell haemoglobin and include sickle cell disorders and thalassaemias. They occur most commonly in populations whose ancestors come from Africa, Asia, Mediterranean Islands, and the Middle and Far East. Haemoglobin (Hb) abnormalities (or haemoglobinopathies) are caused by (i) abnormalities of the protein structure; (ii) imbalanced globin chain production owing to reduced rate of synthesis of normal a or b globin chains; or (iii) a combination of the two. This article will focus on the biological basis of sickle cell disorders and will discuss the history and pathology of the conditions.Entities:
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Year: 2006 PMID: 17077770 DOI: 10.12968/bjon.2006.15.18.22024
Source DB: PubMed Journal: Br J Nurs ISSN: 0966-0461