J Korean Pediatr Soc.  1997 Feb;40(2):260-265.

Erythrocyte Band 7 Integral Protein Defect in Congenital Hemolytic Anemia: Hereditary Stomatocytosis

Affiliations
  • 1Department of Pediatrics, School of Medicine, Hallym University, Chunchon, Korea.
  • 2Department of Genetic Engineering, Hallym University, Chunchon, Korea.

Abstract

Hereditary stomatocytosis is a rare congenital hemolytic anemia, named after mouth shaped or stomatocytic erythrocyte morphology. In this report, we present a case of a hereditary stomatocytosis in a 1 month old boy. During the initial identification process, we overlooked the morphology of the RBC in peripheral blood smear and tentatively diagnosed it to be a hereditary spherocytosis case. In order to study further, we isolated RBC membranes from the patient, separated membrane proteins by SDS polyacrylamide gel electrophoresis, and found that a protein band, band 7, was missing in the patient. We suggest that erythrocyte morphology as well as erythrocyte membrane protein analysis is an important criterion in the diagnosis of hereditary hemolytic anemia.

Keyword

Hereditary stomatocytosis; Membrane protein; Stomatin; SDS-PAGE Deficiency

MeSH Terms

Anemia, Hemolytic, Congenital*
Diagnosis
Electrophoresis, Polyacrylamide Gel
Erythrocyte Membrane
Erythrocytes*
Humans
Infant, Newborn
Male
Membrane Proteins
Membranes
Mouth
Membrane Proteins
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