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Heterogeneity of beta thalassaemia in Thailand.
Southeast Asian J Trop Med Public Health ; 1982 Dec; 13(4): 618-27
Article Dans Anglais | IMSEAR | ID: sea-32227
ABSTRACT
Beta thalassaemia in Thailand is heterogeneous. Clinical, genetical, haematological and globin chain biosynthetic studies were performed in seven beta-thalassaemia families. The results showed different gene combinations. These were alpha-thalassaemia/homozygous beta 0-thalassaemia, questionable double heterozygosity between a beta-thalassaemia and a silent beta-thalassaemia genes with low Hb F of unexplained cause, silent beta-thalassaemia/beta+ - or beta 0-thalassaemia, high Hb A2 high Hb F-beta-thalassaemia - a new mutant, mild beta+-thalassaemia/Hb E, and beta 0-thalassaemia/heterocellular HPFH or delta beta-thalassaemia associated with alpha-thalassaemia. Most of variability of clinical and haematological findings in these families is due to heterogeneity of the beta-thalassaemia and related genes.
Sujets)
Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) Sujet Principal: Pedigree / Thalassémie / Sujet âgé / Femelle / Humains / Mâle / Hémoglobine foetale / Hémoglobine A / Hémoglobine E / Enfant langue: Anglais Texte intégral: Southeast Asian J Trop Med Public Health Année: 1982 Type: Article

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Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) Sujet Principal: Pedigree / Thalassémie / Sujet âgé / Femelle / Humains / Mâle / Hémoglobine foetale / Hémoglobine A / Hémoglobine E / Enfant langue: Anglais Texte intégral: Southeast Asian J Trop Med Public Health Année: 1982 Type: Article