[Not the beta-thalassemia syndrome but hemoglobinopathy H. Studies of 3 clinical cases].
Leo Gc, Paolo Rivasi, De Palma M, E Secchi-Trinelli, G. Milanti, Roberto Silingardi
Abstract
Leo Gc, Paolo Rivasi, De Palma M, E Secchi-Trinelli, G. Milanti, Roberto Silingardi
Abstract
Clinical and laboratory data for three patients are presented. Electrophoretic separation of the freshly obtained haemolysate showed a fast beta-chain fraction on each occasion. This is typical of Hb H disease. The test for erythrocyte inclusion bodies was also positive. The main clinical and haematological features of the disease are illustrated.
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Clinical and laboratory data for three patients are presented. Electrophoretic separation of the freshly obtained haemolysate showed a fast beta-chain fraction on each occasion. This is typical of Hb H disease. The test for erythrocyte inclusion bodies was also positive. The main clinical and haematological features of the disease are illustrated.
Key concepts: Hemoglobinopathy, Beta thalassemia, Thalassemia, Medicine, Disease, BETA (programming language), Internal medicine, Gastroenterology