Doctor insights on:
Beta Thalassemia Medication
How long a spleen pain lasts at a time? Is there any medication b4 start the pain? She is 2 years with beta thalassemia intermedia. Hbn is 8.6 now.
try Ibuprofen: I am assuming that her splenic pain is due to splenic sequestration. Blood may suddenly pool in the spleen. It causes splenic capsule to stretch out causing pain, but also causing her hemoglobin to drop, and may make her very sick. Mild splenic sequestration is tolerable, and for that, one could give Ibuprofen or acetaminophen, but for severe pain, i would recommend a visit to an emergency room. ...Read more
Depends on type...: There are different types of beta thalassemia (minor, intermedia, or major for example) that have much different impacts on a patient's health. Treatment can range from nothing (minor) to requiring frequent blood transfusions, iron chelation therapy or even a bone marrow transplant (major). A hematologist can help with the management of all types. ...Read moreSee 1 more doctor answer
Yes: Thalassemia is one of the most common gene mutations in the world. Overall, an estimated 20-25 million people are carriers (1/300) (about 1/1000 in low-risk peoples, and about 1/30 in high-risk peoples). Low risk: japanese, korean, n. European caucasians, native canadians, native americans. High risk: mediterranean, middle eastern, south asian, south-east asian (western pacific rim), caribbean. ...Read moreSee 1 more doctor answer
No: I am going to assume you have beta thalassemia minor. This is a minor abnormality that makes you trivially anemic and makes your blood cells look a little odd. If you marry someone else who has this, each of your children had 1/4 chance of having thal major, which is a horrible illness. Heads up. Best wishes. ...Read more
What kind?: Beta thal minor shouldn't be a problem. If you have beta thal major and are asking this question, you should be congratulated on your excellent response to treatment and I hope that you get what you want -- but don't be disapponted if you're asked to remain a civilian. ...Read more
Major or minor?: Beta thal minor is a non-problem; the rate of red cell production is somewhat higher so get plenty of Folic Acid in your diet or supplement. Beta thal major is a very serious illness requiring lifelong close management by a physician; again, the need for Folic Acid and a generally nutritious diet is worth remembering but there's no magical food remedy. Good luck. ...Read more
How to know if someone had thalassemia @ beta thalassemia ?What criteria if they had it is dangerous?
I have beta thalassemia and I have hemoglibin d, my fiancee has minor beta thalassemia, is there any problem for our child in future?
My husband and I just received news that we both have beta Thalassemia. He is Caucasian and I'm Indian. What are the chances of our child getting this?
Depends: Thalassemia is autosomal recessive. That means that you only get the disease if you have the gene on both of your chromosome pairs. If you and your husband both have the actual disease, there is a 100% chance your children will have it. If you both have trait (one normal and one disease gene), there is a 25% chance they will have it, and a 50% chance they will be a carrier. I have attached a pic. ...Read more
Yes: Beta thalassemia disease is prevented if beta thal carriers do not have children with one another (if they have children together, some children will be normal, some carriers, and some have disease). The other, less desirable way, is to test fetuses during pregnancy and abort the fetuses who have beta thal major. ...Read moreSee 1 more doctor answer
Unrelated: Beta thal is a congenital disease-where there is defect on the beta- globin inside the rbc. The severity of the disease depends on how many b- globin affected. Beta thal major is very debilitating- tansfusion dependent and only transplant can perhaps cure it. Leukemia however is malignancy of the progenitors of the white cells-in bone marrow. Different types of leukemia-acute vs chronic leukemia. ...Read moreSee 1 more doctor answer
Similar but differen: Alpha and beta thalassemia are distinct and different disorders since they diminish the production of distinct and different globin polypeptide chains and particularly in the homozygous state that has distinct and different consequences. Alpha and Beta Thal minor are similar Alpha Thal major is not compatable with life and results in miscarriage. Beta Thal major requires prolonged treatments etc. ...Read more
For those who having hb e/beta thalassemia, what food should they eat and what should not they eat?
Thalassemia : This is a genetic hemolytic blood disorders transmitted to you from your parents in your genes & instead of having the normal Hgb A, it becomes abnormal Hgb. there are different types of thalassemia. If both parents are carriers or have the disease then the offspring might get the disease. I hope this helps. Good luck. ...Read more
- Talk to a doctor live online for free
- Delta beta thalassemia
- Hemoglobin's beta thalassemia
- Beta thalassemia trait diagnosis
- Ask a doctor a question free online
- Beta thalassemia major symptoms
- Beta thalassemia major treatment
- Major beta thalassemia
- Beta thalassemia intermedia
- Beta thalassemia