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Various forms of beta-thalassemia among children of Azerbaĭjan

Rustamov, R.Sh.; Dadasheva, T.S.; Limborskaia, S.A.

Problemy Gematologii i Perelivaniia Krovi 26(9): 3-7

1981

ISSN/ISBN: 0552-2080
PMID: 6458807
Document Number: 172450
According to varying .beta.-thalassemia genes synthesized in 51 homozygotes and 109 heterozygotes, 4 forms of .beta.-thalassemia were distinguished: .beta.-thalassemia major by the gene of classic .beta.-thalassemia (which in the minor state is characterized by an HbA2 increase); .beta.-thalassemia major by the gene of silent .beta.-thalassemia (which in the minor state does not induce an HbA2 increase); .beta.-thalassemia caused by combined genes of classic and silent .beta.-thalassemia; .beta.-thalassemia for which combined genes of .delta.beta.- and classic .beta.-thalassemia are responsible. The carriership of the silent .beta.-thalassemia gene in the Azerbaijan population described for the 1st time and its high frequency was discussed.

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