Ontology highlight
ABSTRACT:
SUBMITTER: Swe KM
PROVIDER: S-EPMC9964104 | biostudies-literature | 2013 Jun
REPOSITORIES: biostudies-literature
Swe Kye Mon Min KM Abas Adinegara B L AB Bhardwaj Amit A Barua Ankur A Nair N S NS
The Cochrane database of systematic reviews 20130628 6
<h4>Background</h4>Haemoglobinopathies, inherited disorders of haemoglobin synthesis (thalassaemia) or structure (sickle cell disease), are responsible for significant morbidity and mortality throughout the world. The WHO estimates that, globally, 5% of adults are carriers of a haemoglobin condition, 2.9% are carriers of thalassaemia and 2.3% are carriers of sickle cell disease. Carriers are found worldwide as a result of migration of various ethnic groups to different regions of the world. Zinc ...[more]