Red cells I: inherited anaemias

Citation
Dj. Weatherall et Ab. Provan, Red cells I: inherited anaemias, LANCET, 355(9210), 2000, pp. 1169-1175
Citations number
26
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
LANCET
ISSN journal
01406736 → ACNP
Volume
355
Issue
9210
Year of publication
2000
Pages
1169 - 1175
Database
ISI
SICI code
0140-6736(20000401)355:9210<1169:RCIIA>2.0.ZU;2-0
Abstract
Examination of the genetic mechanisms underlying the thalassaemias has led to a clearer understanding of the control of eukaryotic genes in general. Inherited disorders of haemoglobin synthesis are an important cause worldwi de of morbidity and mortality, and place a large burden on patients, famili es, and ultimately communities. The haemoglobin disorders can be controlled, by counselling and prenatal di agnosis. Treatment is usually symptomatic, though bone-marrow transplantation for be ta-thalassaemia may be successful in suitable patients.