Treatment that can be given to thalassemia patient
A. Stem cell or bone marrow transplant
B. Blood transfusions
C. Iron chelation
D. All of these
Answer
396.6k+ views
Hint:
Thalassemia is a genetically transmitted (i.e., handed from parents to children) blood illness that develops when the body doesn't produce enough haemoglobin, a crucial component of red blood cells. Fewer healthy red blood cells are moving through the bloodstream when haemoglobin levels are low because the body's red blood cells don't work correctly and live for shorter periods.
Complete answer:
There are a few different treatments that can be given to thalassemia patient Stem cell or bone marrow transplant, Blood transfusions, and Iron chelation depending on the individual's specific situation.
For patients with stem cell therapy, this procedure may involve infusing new stem cells into the bloodstream in order to replace those that have been damaged or destroyed. This is often considered a more permanent treatment and has a high success rate.
Additionally, if a person has undergone a bone marrow transplant, then their body will likely produce enough white blood cells (WBCs) to fight off infections and disease. Those who require regular WBC transfusions may find relief by taking iron supplements before their Transfusion in order to help improve their Lymphocyte function.
And lastly, for people who experience anaemia due to Thalassemia trait, oral clotting factor concentrates could be administered regularly through diet or intravenous infusion in order to increase haemoglobin levels back up until they reach normal ranges again.
Option ‘D’ is correct
Note:
Patients with thalassemia who require bone marrow or stem cell transplants, blood transfusions, or iron chelation may get one of several possible treatments. The optimal choice may change depending on the particular circumstance. To help a person with this illness, however, improve their overall health and well-being, often all of these treatments are required.
Thalassemia is a genetically transmitted (i.e., handed from parents to children) blood illness that develops when the body doesn't produce enough haemoglobin, a crucial component of red blood cells. Fewer healthy red blood cells are moving through the bloodstream when haemoglobin levels are low because the body's red blood cells don't work correctly and live for shorter periods.
Complete answer:
There are a few different treatments that can be given to thalassemia patient Stem cell or bone marrow transplant, Blood transfusions, and Iron chelation depending on the individual's specific situation.
For patients with stem cell therapy, this procedure may involve infusing new stem cells into the bloodstream in order to replace those that have been damaged or destroyed. This is often considered a more permanent treatment and has a high success rate.
Additionally, if a person has undergone a bone marrow transplant, then their body will likely produce enough white blood cells (WBCs) to fight off infections and disease. Those who require regular WBC transfusions may find relief by taking iron supplements before their Transfusion in order to help improve their Lymphocyte function.
And lastly, for people who experience anaemia due to Thalassemia trait, oral clotting factor concentrates could be administered regularly through diet or intravenous infusion in order to increase haemoglobin levels back up until they reach normal ranges again.
Option ‘D’ is correct
Note:
Patients with thalassemia who require bone marrow or stem cell transplants, blood transfusions, or iron chelation may get one of several possible treatments. The optimal choice may change depending on the particular circumstance. To help a person with this illness, however, improve their overall health and well-being, often all of these treatments are required.
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