A Case of Familial beta-thalassemia Minor
Journal of the Korean Pediatric Society
;
: 557-560, 1995.
Article
Dans Coréen
| WPRIM
| ID: wpr-197065
ABSTRACT
Thalassemias are a diverse group of inherited anemias that are characterized by defective synthesis of one or more globin chains. The thalassemias are classified according to the globin chain or chains the synthesis of which is deficient alpha-, beta-, delta beta-, delta-, and gamma delta beta- Thalassemia. They are common in the Mediterranean region, The Middle East, India, Burma, and Southeast Asia. Beta-thalassemia minor, the heterozygous state, is most frequently characterized by hypochrmia, microcytosis and an elevated percentage of hemoglobin A2. We experienced a case of a familial beta-thalassemia minor in pneumonia patient and his family.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Pneumopathie infectieuse
/
Asie du Sud-Est
/
Thalassémie
/
Globines
/
Hémoglobine A2
/
Bêta-Thalassémie
/
Myanmar
/
Région méditerranéenne
/
Inde
/
Anémie
Limites du sujet:
Humains
Pays comme sujet:
Asie
/
Europe
langue:
Coréen
Texte intégral:
Journal of the Korean Pediatric Society
Année:
1995
Type:
Article
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