Beta thalassemia is a blood disorder where there is abnormal hemoglobin production. It is caused due to mutation in the hemoglobin beta gene. There are three types of beta-thalassemia. They are beta thalassemia minor, beta thalassemia intermedia, and beta thalassemia major. Depending on the type of beta-thalassemia, the symptoms can be minor or severe. The signs and symptoms are shortness of breath, pale skin, tiredness, increased heart rate, and yellowish discoloration of eyes and skin. Taking regular blood transfusions along with medications helps to manage it.
Hi, Welcome to icliniq.com. Your attached CBC report shows normal hemoglobin and MCV, and the RBC count is also within range (attachment removed to protect patient identity).
Hello, Welcome to icliniq.com. Beta thalassemia major is a hereditary disorder and is due to a genetic deficiency of beta globin chains of hemoglobin. It is transfusion-dependent anemia.
Hi, Welcome to icliniq.com. Thank you for your query. Based on the information provided, here is my professional opinion: Low hemoglobin levels can have various causes.
Hello, Welcome to icliniq.com. As per your description, your friend seems to be having sickle beta-thalassemia.
Hello, Welcome to icliniq.com. I have seen the reports (attachment removed to protect patient identity). Thalassemia and sickle cell anemia are autosomal recessive disorders.
Hello, Welcome to icliniq.com. I read your query and understand your concern.
Hello, Welcome to icliniq.com. As your child is suffering from thalassemia intermedia, you should avoid giving iron-rich food and food that leads to an increase in iron absorption.
Hi, Welcome to icliniq.com. Based on your query, my opinion is as follows: Thalassemia is a disease due to reduced globin production in the hemoglobin part of RBC (red blood cells).
Hi, Welcome to icliniq.com. Based on your query, my opinion is as follows: The beta-thalassemia screening test appears to be normal. HbA2 levels (hemoglobin A2) are normally between 2 to 3.
Hello,Welcome to icliniq.com.Your attached report (attachment removed to protect patient identity) is suggestive of a sickle cell plus beta thalassemia combination case.
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