From: Chapter 1, EPIDEMIOLOGY, PATHOPHYSIOLOGY AND DIAGNOSIS OF α-THALASSAEMIA
NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.
Peripheral blood smears of patients with HbH disease typically exhibit variable degrees of microcytic hypochromic anaemia, a distinctive feature of this condition. Figure 6 illustrates several haematological anomalies commonly observed in individuals with HbH disease, including severe hypochromia, anisocytosis (variation in cell size), poikilocytosis (abnormal cell shapes), microcytosis (small cell size), fragmentation, anisochromia (variation in cell colour), polychromasia (presence of polychromatic cells), target cells, and teardrop cells.
From: Chapter 1, EPIDEMIOLOGY, PATHOPHYSIOLOGY AND DIAGNOSIS OF α-THALASSAEMIA
NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.