J Korean Pediatr Soc.  1995 Apr;38(4):557-560.

A Case of Familial beta-thalassemia Minor

Affiliations
  • 1Department of Pediatrics and Clinical Pathology, St. Columban Hospital, Mokpo, Korea.

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.

Keyword

beta-thalassemia minor

MeSH Terms

Anemia
Asia, Southeastern
beta-Thalassemia*
Globins
Hemoglobin A2
Humans
India
Mediterranean Region
Middle East
Myanmar
Pneumonia
Thalassemia
Globins
Hemoglobin A2
Full Text Links
  • KJP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr