| Literature DB >> 9161189 |
M S Duggal1, R Bedi, S E Kinsey, S A Williams.
Abstract
This paper reviews two groups of haemoglobinopathies: sickle cell disorders and beta-thalassaemias. The medical aspects and dental management of children with these conditions are discussed. These conditions are rare in the white indigenous population of the UK but affect a sizeable proportion of the minority ethnic community. Dentists need to be aware of the medical implications for patients who have these disorders and should co-ordinate their dental care accordingly.Entities:
Mesh：
Year: 1996 PMID： 9161189 DOI： 10.1111/j.1365-263x.1996.tb00250.x
Source DB: PubMed Journal: Int J Paediatr Dent ISSN： 0960-7439 Impact factor: 3.455