Laboratory Findings in Beta Thalassemia

Hematologic Findings For Various Types of Beta Thalassemia

Beta Thalassemia Silent Carrier

Beta Thalassemia Minor Beta Thalassemia Intermedia Beta Thalassemia Major

Delta-Beta Thalassemia

Anemia Absent Mild to absent Moderate Severe Mild

Red blood cell (RBC) count

Normal Increased Decreased to normal Decreased Decreased to normal

Hemoglobin(Hb)

Normal Decreased to normal (10 - 12 g/dL) Decreased (7 - 10 g/dL) Marked decrease (<7 g/dL)

Decreased to normal (8 - 13 g/dL)

Mean corpuscular volume (MCV) Slight to no decrease Marked decrease Marked decrease Marked decrease May be slightly decreased
Mean corpuscular hemoglobin concentration (MCHC) Slight to no decrease Marked decrease Marked decrease Marked decrease May be slightly decreased
Red blood cell distribution width (RDW) Normal Normal to slightly increased Increased Increased Normal
RBC morphology Normal
  • Marked hypochromia and microcytosis
  • Codocytes (target cells)
  • Possible basophilic stippling

Nucleated RBCs are usually not present

  • Marked hypochromia and microcytosis
  • Codocytes (target cells)
  • Possible basophilic stippling

Nucleated RBCs are usually not present

  • Marked hypochromia and microcytosis
  • Codocytes (target cells)
  • schistocytes
  • ovalocytes
  • basophilic stippling
  • polychromasia
  • nucleated RBCs
  • Possible hypochromia and microcytosis
  • Codocytes (target cells)
  • Basophilic stippling
Reticulocyte count Normal May be slightly increased Slightly increased (<5%) Mildly increased (5 - 10%) Mildly increased
Hb electrophoresis Normal pattern
  • Decreased amount of Hb A
  • Variable amounts of Hb A2 and Hb F
  • Decreased amount of Hb A
  • Variable amount of Hb A2
  • Hb F is usually increased
  • Severly decreased amount of Hb A
  • Variable amount of Hb A2
  • Usually an increased amount of Hb F

Decreased amount of Hb A and Hb A2

Increased amount of Hb F (15 - 20%)

If red blood cells are normochromic and normocytic, the RBC, Hb, and Hematocrit (HCT) test values follow in three-fold progression (i.e., RBC x 3 = Hb and Hb x 3 = HCT). This is sometimes referred to as "the rule of threes." This rule will usually not apply in cases of beta thalassemia, particularly beta thalassemia minor where the RBCs are not normochromic and are microcytic, and where there is a disproportionate number of RBCs for the amount of hemoglobin that is present.

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