Further Cases of Hb Q-H Disease (Hb Q-α Thalassemia)
| Autor: | V. Thuraisingham, Lie-Injo Luan Eng, R. P. Pillay |
|---|---|
| Rok vydání: | 1966 |
| Předmět: |
medicine.medical_specialty
Blood transfusion business.industry medicine.medical_treatment Thalassemia Immunology Hepatosplenomegaly Cell Biology Hematology Jaundice medicine.disease Haemolysis Biochemistry Endocrinology Internal medicine Hypochromia medicine Anisocytosis Hemoglobin medicine.symptom business |
| Zdroj: | Blood. 28:830-839 |
| ISSN: | 1528-0020 0006-4971 |
| DOI: | 10.1182/blood.v28.6.830.830 |
| Popis: | Case reports of four patients, all Chinese, with Hb Q-H disease—also called Hb Q-α thalassemia—are presented. Three were siblings. Symptoms of chronic hemolytic anemia with jaundice and hepatosplenomegaly were present in all four subjects. The red blood cells were microcytic. Slight hypochromia was present in three of the cases. Poikilo- and anisocytosis with target cells and small intraerythrocytic crystals were found in the blood. Starch-gel electrophoresis revealed the presence of a large amount of Hb Q, a small amount of Hb H, and a minor slow-moving hemoglobin component with a mobility as much behind Hb A2 as Hb Q was behind Hb A. A small amount of Hb "Bart’s" was probably also present. The minor slow-moving component was thought to represent Hb α2Qδ2A2 or Hb Q2. Hb A and Hb A2 were not seen except after recent blood transfusion. Study of hemoglobin polypeptide chains showed the presence of normal βA-chains and abnormal αQ-chains, without demonstrable αA-chains in the first three patients. In Patient #4 normal αA-chains were demonstrable only after recent blood transfusion. The mother of the three siblings was heterozygous for Hb A; the father had α-thalassemia trait. |
| Databáze: | OpenAIRE |
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