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Blood, 1970, Vol. 35, No. 2, pp. 158-165.
© 1970 American Society of Hematology, Inc.

A Family with Three betadgr-Thalassemia Homozygotes

BRACHA RAMOT 1, ISAAC BEN-BASSAT 1, DOROTHEA GAFNI 1, and REYAD ZAANOON 1

1 Department of Hematology, Tel-Hashomer Government Hospital and Tel-Aviv University Medical School and Medical Section, Shifa Government Hospital, Gaza, Israel.

An Arab family with three homozygotes for betadgr-thalassemia is described. The single hemoglobin present in their red cells is fetal hemoglobin. A mild hemolytic condition was seen in the propositus, while the two other siblings are completely normal. The main differential diagnosis of this condition is homozygosity for persistent fetal hemoglobin gene.

Submitted on June 18, 1969
Accepted on August 27, 1969


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