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[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

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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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What this paper is about

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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Available 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.

Key concepts: Hemoglobinopathy, Beta thalassemia, Thalassemia, Medicine, Disease, BETA (programming language), Internal medicine, Gastroenterology

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[Not the beta-thalassemia syndrome but hemoglobinopathy H. Studies of 3 clinical cases]. — Research Paper | ScholarLens