Purpose of the Screening
- Detection of Sickle Cell Anemia and Thalassemia.
- Quantifying normal and abnormal hemoglobin variants.
- Diagnosing causes of hereditary anemia.
Book Hemoglobin Electrophoresis | Lahalak Medical Platform
Identify hemoglobin variants in your blood for early detection of Sickle Cell Anemia and Thalassemia. This essential screening helps in health planning and preventing hereditary complications for you and your family.
Scientific name: Hemoglobin Electrophoresis Screening
A precise laboratory test to separate and quantify hemoglobin variants (HbA, HbS, HbF, HbA2). It diagnoses hereditary blood disorders and identifies carriers to ensure a healthy future.
Service type
Laboratory test
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Venous blood sample collection
- Hemoglobin separation analysis
- Detailed medical report
Medical Service Information
Target Groups
- Couples planning for marriage (Pre-marital screening).
- Individuals with a family history of blood disorders.
- Patients with chronic unexplained anemia.
Significance of Results
- Identifies whether a person is a carrier or affected by the disease.
- Helps reduce the spread of genetic diseases to future generations.
- Guides physicians in choosing the appropriate treatment for anemia.
Conditions & Notices
- Please inform the lab if you had a blood transfusion in the last 3 months.
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