Acquired alpha-thalassemia as early sign for myelodysplastic syndrome (refractory anaemia) with secondary haemochromatosis

We report the case of a 59 year old man presenting a regenerative microcytic hypochromic anaemia. The investigations revealed the presence of haemoglobin H, suggesting abnormalities in the alpha-globin chains synthesis. Alpha-thalassemia was thus suspected. The patient had no personal or familial hi...

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Veröffentlicht in:	Annales de biologie clinique (Paris) 2007-07, Vol.65 (4), p.405-409
Hauptverfasser:	Perrin, J, Perrot, A, Chenot, V, Lesesve, J-F, Guerci, A, Marchand-Arvier, M, Vigneron, C, Lecompte, T
Format:	Artikel
Sprache:	fre
Schlagworte:	alpha-Thalassemia - etiology alpha-Thalassemia - pathology Anemia, Refractory - diagnosis Anemia, Refractory - pathology Erythrocytes - pathology Hemochromatosis - diagnosis Hemochromatosis - pathology Humans Male Middle Aged Myelodysplastic Syndromes - diagnosis Myelodysplastic Syndromes - pathology
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