A New Thalassemic Syndrome: Homozygous Hemoglobin S Disease Delta Thalassemia
- 1 January 1966
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 36 (5-6) , 412-417
- https://doi.org/10.1159/000209421
Abstract
A case of homozygous Hb-S delta thalassemia is presented. The genetic inheritance of the genes is discussed and related to the family pedigree. Observations regarding other genetic combinations are also presented and discussed. It is apparent that this combination presents a mild hemolytic disease.Keywords
This publication has 3 references indexed in Scilit:
- The First Observation of Homozygous Hemoglobin S-Alpha Thalassemia Disease and Two Types of Sickle Cell Thalassemia Disease: (a) Sickle Cell-Alpha Thalassemia Disease, (b) Sickle Cell-Beta Thalassemia DiseaseBlood, 1963
- Genetic Basis of the Thalassæmia DiseasesNature, 1959
- Solubilities of naturally occurring mixtures of human hemoglobinArchives of Biochemistry and Biophysics, 1953