Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Base de dados
Assunto principal
Intervalo de ano de publicação
1.
Ann Pediatr (Paris) ; 37(7): 455-7, 1990 Sep.
Artigo em Francês | MEDLINE | ID: mdl-1701619

RESUMO

We report two cases of intermediate beta-thalassemia diagnosed at the age of 2 years and 3 1/2 years respectively. Characteristic features of this disease include delayed onset, moderate blood transfusion requirements, and frequent development of hypersplenism. Major iron overload develops even in patients who have received no transfusions. This disease is further characterized by significant genetic heterogeneity and by a reduction in the imbalance between produced chains and deficient chains.


Assuntos
Talassemia/diagnóstico , Pré-Escolar , Consanguinidade , Hemoglobina Fetal/análise , Hemoglobina A/análise , Hemoglobina A2/análise , Humanos , Masculino , Prognóstico , Talassemia/sangue , Talassemia/genética , Tunísia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA