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Is the beta thalassaemia trait of clinical importance?
Premawardhena, A; Arambepola, M; Katugaha, N; Weatherall, D J.
Affiliation
  • Premawardhena A; Faculty of Medicine, University of Kelaniya, Colombo, Sri Lanka. anuja@mfac.kln.ac.lk
Br J Haematol ; 141(3): 407-10, 2008 May.
Article in En | MEDLINE | ID: mdl-18341640
Although the beta thalassaemia trait affects millions of people worldwide, there have been no controlled studies to determine whether it is associated with any clinical disability or abnormal physical signs. To address this question, 402 individuals were studied: 217 with beta thalassaemia trait, of whom 154 were aware of the diagnosis and 63 were unaware until after the completion of the study; 89 normal controls; and 96 controls with mild hypochromic anaemia. There was a significant increase in symptoms ascribable to anaemia and episodes of pyrexia in those with the beta thalassaemia trait that were not influenced by prior knowledge that they had this condition. There was no difference in physical findings, notably splenomegaly, between those with beta thalassaemia trait and either control group.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beta-Thalassemia / Heterozygote Type of study: Etiology_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Br J Haematol Year: 2008 Document type: Article Affiliation country: Sri Lanka Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beta-Thalassemia / Heterozygote Type of study: Etiology_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Br J Haematol Year: 2008 Document type: Article Affiliation country: Sri Lanka Country of publication: United kingdom