Thalassemia is a genetic blood disorder characterized by abnormal production of hemoglobin, the protein in red blood cells that carries oxygen. Individuals with thalassemia produce fewer healthy red blood cells and less hemoglobin than normal, leading to anemia. Thalassemia can range from mild to severe forms, depending on the specific genetic mutations involved. Symptoms may include fatigue, weakness, pale skin, jaundice, and growth delays, among others. Treatment includes blood transfusions and iron chelation therapy.

Am I At The Risk For Having Thalassemia?

Yes 

Have you been diagnosed with blood disorders?

Do you have a family history of thalassemia or related blood disorders? 

Have you ever been diagnosed with persistently low hemoglobin levels? 

Have you previously received blood transfusions or iron chelation therapy (removal of excessive iron from blood)? 

Do you experience fatigue or weakness, particularly after exertion? 

Have you noticed any changes in the color of your skin or eyes (jaundice)? 

Do you have frequent headaches or dizziness? 

Have you experienced shortness of breath or chest pain? 

Do you have a history of leg swelling or abdominal discomfort? 

Have you ever been diagnosed with bone disorder (thin bones, frequent fractures)? 

Do you experience any limitations in physical activities due to your condition? 

Yes   

Have you experienced symptoms such as fatigue, weakness, or abdominal pain? 

Have you ever been screened for complications associated with thalassemia, such as iron overload, bone abnormalities, or heart problems? 

Have you experienced any symptoms such as joint pain, frequent infections, or abnormal heart rhythms? 

Are you currently planning to start a family or have you considered genetic counseling? 

Are you aware of the genetic implications of thalassemia for your future children? 

Have you ever been diagnosed with an enlarged spleen? 

A low score in Thalassemia assessment typically presents with few or no symptoms however, even with a mild score, regular monitoring and medical care are important to ensure proper management and prevent potential complications over time. 

LOW: Low Risk 

Moderate Thalassemia usually requires regular monitoring and may necessitate occasional blood transfusion or other supportive treatments and regular evaluation by your doctor. 

MODERATE: Moderate Risk

Severe thalassemia is characterized by more pronounced symptoms and complications, often requiring frequent blood transfusion, chelation therapy to manage iron overload, and others, and may require hospital-based treatments. 

HIGH: High Risk

Am I At The Risk For Having Thalassemia?

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