Doctor insights on:
What Are The Treatments Available For Beta Thalassemia
Blood transfusions: Beta thalassemia trait patients are non-anemic or mildly anemic, and they do not need treatment. Beta thalassemia intermedia patients have anemia, and sometimes they are severe enough to need occasional transfusions. Beta thalassemia major (cooley's anemia) patients are dependent on lifelong transfusions to survive, and they will eventually suffer from iron overload. ...Read moreSee 1 more doctor answer
I was diagnosed with heterozygous beta thalassemia . My iron levels was 6. This concerned me. Friend said iron treatment i'll get sick? What to do?
I'm a bit skeptical: I find it surprising that a diagnosis of beta thal trait could have gone undiscovered for 37 years. Moreover, in the context of fe deficiency (which is suggested by a serum fe of 6), you can't definitively diagnose beta-thal trait. In an fe replete state, beta thal trait is suggested by a hemoglobin a2 (alpha2/delta2) of >3.5% i would correct the fe deficiency, then repeat the hgba2 quantitation. ...Read moreSee 2 more doctor answers
What i need to do once i had diagnose "beta thalassemia" by doctor? What treatment I should do? Please help me doctor..
Nothing: If you were just diagnosed with beta thalassemia at age 26, you must have the "minor" form, beta-thalassemia trait. You most likely have mild microcytic anemia that has been present all of your life. The only issue is that if your partner has beta-thalassemia trait, then you could have a child with severe transfusion-dependent beta-thalassemia major. ...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
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
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
Pediatric Hematolo-: gists have the expertise to diagnose & treat Hb E/?-thalassaemia, which results from co-inheritance of a ?-thalassaemia allele, an alternative form of a gene, from 1 parent and the structural variant Hemoglobin E from the other. They check for co-inheritance of ?-thalassemia & polymorphisms, 2 or more alleles at 1 locus, that ^ synthesis of Fetal Hb. These are factors that determine severity. ...Read more
Genetic disorder: http://www.ncbi.nlm.nih.gov/pmc/articles/pmc3237252/ "the disorder is characterized by marked clinical variability, ranging from a mild and asymptomatic anaemia to a life-threatening disorder requiring transfusions from infancy. "...."careful tailoring of treatment is required for each patient, and that therapeutic approaches should be re-assessed over-time." not curable..Look at website-. ...Read more
Anemia symptoms: The symptoms of beta thalassemia major are those of severe anemia, which include weakness, pallor (pale appearance), decreased growth/development, rapid heart rate, exercise intolerance, thickened bones as the marrow enlarges to try to make more blood cells, enlarged spleen, etc... ...Read moreSee 1 more doctor answer
Manifestations vary: Hgb e/b-t results from inheritance of a HGB e mutation from one parent and a beta-thalassemia mutation from the other parent. The severity of HGB e/b-t varies from mild to severe. ~50% of individuals who have HGB e/b-t have severe manifestations that resemble thalassemia major. ~50% of individuals who have HGB e/b-t have symptoms similar to thalassemia intermedia. ...Read more
Yes: It's a horrible disease but the newer remedies are helping these folks live longer and better. ...Read more
- Talk to a doctor online
- Alternative treatments for beta thalassemia
- What treatments are available for prostate cancer?
- What are the different breathing treatments that are available?
- What are the treatments available for kidney stones?
- What treatments are available for heart disease?
- What are available treatments for a prolapsed bladder?
- What treatments are available for nocturnal migraines?
- Beta thalassemia
- Treatments for beta thalassemia minor