Etiology, investigations, and differential diagnosis of microcytic hypochromic anemia
Thalassemia syndromes: Types, genetic basis, and diagnostic criteria
Microcytic hypochromic anemia is caused by various factors including iron deficiency and genetic disorders like thalassemia. Proper investigations and differential diagnosis help in effective management.
Etiology, Investigations, and Differential Diagnosis of Microcytic Hypochromic Anemia
Introduction
Microcytic hypochromic anemia is characterized by small and pale red blood cells. It often results from iron deficiency, chronic diseases, or genetic conditions such as thalassemia syndromes.
Etiology
The primary causes of microcytic hypochromic anemia include:
- Iron deficiency anemia
- Thalassemia syndromes
- Anemia of chronic disease
- Sideroblastic anemia
Investigations
Diagnosis involves laboratory tests such as:
- Complete blood count (CBC)
- Serum iron studies
- Hemoglobin electrophoresis
- Genetic testing for thalassemia
Thalassemia Syndromes
Thalassemia is a genetic disorder affecting hemoglobin production. It is classified into:
- Alpha thalassemia
- Beta thalassemia
Diagnosis relies on hematological tests and genetic analysis.
Differential Diagnosis
Conditions mimicking microcytic hypochromic anemia include:
- Lead poisoning
- Chronic infections
- Hemolytic anemia
Conclusion
Accurate diagnosis is critical for effective management of microcytic hypochromic anemia and its underlying conditions.
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