Hematological and hemoglobin synthesis studies in a family with deltabeta-thalassemia trait.
Acta Haematol
; 61(1): 27-32, 1979.
Article
em En
| MEDLINE
| ID: mdl-105537
ABSTRACT
A Basque Spanish family with heterozygous deltabeta-thalassemia is described. Patients with this anomaly usually present hematological findings observed in classical beta-thalassemia, but clinical conditions and unbalanced chain synthesis are less severe. Our propositus, however, presented clinical and biosynthetic data similar to those described in thalassemia intermedia. A family study was also performed.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Talassemia
/
Hemoglobinas
Limite:
Adolescent
/
Adult
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
País/Região como assunto:
Europa
Idioma:
En
Revista:
Acta Haematol
Ano de publicação:
1979
Tipo de documento:
Article