| Literature DB >> 10791394 |
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 worldwide of morbidity and mortality, and place a large burden on patients, families, and ultimately communities. The haemoglobin disorders can be controlled, by counselling and prenatal diagnosis. Treatment is usually symptomatic, though bone-marrow transplantation for beta-thalassaemia may be successful in suitable patients.Entities:
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Year: 2000 PMID: 10791394 DOI: 10.1016/s0140-6736(00)02073-0
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321