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Hemoglobin S Beta Thalassemia Disease
Sign/Symptoms
Anaemia (Anemia)
Blood: Microcytic Anemia
Blood: Sickle Cell Anemia
Drugs
Our Records are Incomplete for Drugs
Treatments
Attributes
Cause
= Genetic
Commonality
is
rare
Further Tests
Chorionic Villus Sampling (CVS)
Abnormal Genetic or Biochemical Markers (Increased)
Erythrocyte Fragility Test (Osmotic Fragility, OF)
Percentage NaCl at which Hemolysis begins (Decreased)
Percentage NaCl at which Hemolysis is complete (Decreased)
Fetal Hemoglobin (Hemoglobin F, HbF) Concentration
Fetal Hemoglobin (Hemoglobin F, HbF) (Increased)
Free Erythrocyte Protoporphyrin (FEP) Concentration
Free Erythrocyte Protoporphyrin (FEP) (Increased)
Glycosylated Hemoglobin (HbA1c) Concentration
haptoglobin (Hp) concentration
haptoglobin (Hp) (Decreased)
Heinz Stain
Heinz Bodies (Increased)
Hemoglobin (Hb) A2 Concentration
Hemoglobin (Hb) A2 (Increased)
Hemoglobin S Concentration (Sickle Cell Test)
Hemoglobin S (Increased)
Iron Concentration
Iron (Increased)
Mean Corpuscular Hemoglobin (MCH) Weight Test
Hemoglobin (Hb) (Decreased)
Mean Corpuscular Hemoglobin Concentration (MCHC)
Hemoglobin (Hb) (Decreased)
Mean Corpuscular Volume (MCV)
Red Blood Cell (RBC) Volume (Decreased)
Red Blood Cell (RBC) Count
Red Blood Cells (RBC) (Increased)
Reticulocyte Absolute Count
Reticulocytes (Increased)
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