Red cells II: acquired anaemias and polycythaemia

Citation
D. Provan et D. Weatherall, Red cells II: acquired anaemias and polycythaemia, LANCET, 355(9211), 2000, pp. 1260-1268
Citations number
43
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
LANCET
ISSN journal
01406736 → ACNP
Volume
355
Issue
9211
Year of publication
2000
Pages
1260 - 1268
Database
ISI
SICI code
0140-6736(20000408)355:9211<1260:RCIAAA>2.0.ZU;2-T
Abstract
Iron deficiency affects 30% of the world's population. Iron metabolism is tightly regulated, with both gut transport and storage b eing coordinated. Hereditary haemochromatosis due to mutations in the HFE gene loads to incre ased absorption of iron and multiple end-organ damage. Myelodysplastic disorders are acquired clonal stem-cell disorders that caus e ineffective erythropoiesis. Aplastic anaemia is caused by an intrinsic defect of haemopoietic stem cell s; both inherited and acquired forms occur. Primary polycythaemia is a myeloproliferative disorder, a non-malignant ste m-cell disease.