Thalassemia Beta globin gene sequencing Questions

Abir hbe thalassemia, hb 6.9 wbc 10300, plate late 512000, uses folvite cal 500 hydrox urea 500. After stopping 60 days hydrox urea plate increase more than 300000. How it can be decreased?

Diploma in Gastroenterology, Diploma In Pulmonary Medicine , MSCP, BHMS, SVD( Skin & Veneral Diseases)
Homeopathy Doctor, Hyderabad
Abir hbe thalassemia, hb 6.9 wbc 10300, plate late 512000, uses folvite cal 500 hydrox urea 500. After stopping 60 da...
In thalassemia, managing blood parameters is complex and requires regular medical supervision. While homeopathy can support general well-being, it's critical for you to continue consulting with a me. Remedies like ferrum phos and calcarea phos might be helpful, but professional medical advice is indispensable.
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Hi … good afternoon doctor. I have thalassemia intermediate. I am doing my treatment from pgi. And I also want to meet you regarding my problem. If you need and latest test reports, please text me. And also send me you address. Because I booked appointment and don’t know your address. Thanks.

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow Of Academy Of General Education (FAGE), DNB, Fellowship in Critical Care Medicine, ATLS(Advanced trauma life support )
General Physician, Delhi
Hi … good afternoon doctor. I have thalassemia intermediate. I am doing my treatment from pgi. And I also want to mee...
I am sorry to hear about your concern but will be happy to assist you let's connect over a call so that we can discuss your concern in details and make a treatment plan for you.
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I'm having beta thalassemia minor but my parents are normal is it possible? If not what is the reason.

Ph-9477246755 Fee-2000 Rs
Homeopathy Doctor, Kolkata
I'm having beta thalassemia minor but my parents are normal is it possible? If not what is the reason.
Yes it is possible parents negative but they are carrier of thalassemia genes which will transfer to their child and thalassemia positive happen.
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Is there possible to bone marrow transplantation in thalassemia patients after spleen operation (spleen removals operation) please answer answer anybody as soon as possible.

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow of Academy of General Education (FAGE)
General Physician, Delhi
Is there possible to bone marrow transplantation in thalassemia patients after spleen operation (spleen removals oper...
I am sorry to hear about your concern but will be happy to assist you. The overall thalassemia-free survival of low-risk, hla-matched sibling stem cell transplantation patients is 85 to 90 percent, with a 95 percent overall survival. While not as effective, new approaches to class 2 and 3 patients have significantly improved their overall survival. Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.
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My son suffering thalassemia major. My son 6 year old and last 5 year blood transfusion after 20 day.

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow of Academy of General Education (FAGE)
General Physician, Delhi
My son suffering thalassemia major. My son 6 year old and last 5 year blood transfusion after 20 day.
I am sorry to hear about your concern but will be happy to assist you. Most people with thalassaemia major or other severe types will need to have regular blood transfusions to treat anaemia. This involves being given blood through a tube inserted into a vein in your arm. It's usually done in hospital and takes a few hours each time. Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.
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What is beta thalassemia? How long can live a beta thalassemia patient? What to do to cure thalassemia? Is beta thalassemia is genetic disorder?

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow of Academy of General Education (FAGE)
General Physician, Delhi
What is beta thalassemia?
How long can live a beta thalassemia patient?
What to do to cure thalassemia?
Is beta thala...
I am sorry to hear about your concern but will be happy to assist you. Beta thalassemia is an inherited blood disorder characterized by reduced levels of functional hemoglobin. Hemoglobin is found in red blood cells; it is the red, iron-rich, oxygen-carrying pigment of the blood. A main function of red blood cells is to deliver oxygen throughout the body. Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.
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I am 24 women who has minor alpha thalassemia trait am also having who is also overweight. Currently after taking pfizer vaccine second dose, my blood pressure is 76/44 78. After taking pfizer vaccine, I am slight feeling under weather like fatigue and some slight chest pain, fatigue.my thyroid is normal according to my blood result.

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow of Academy of General Education (FAGE)
General Physician, Delhi
I am 24 women who has minor alpha thalassemia trait am also having who is also overweight. Currently after taking pfi...
I am sorry to hear about your concern but will be happy to assist you fatigue can be a less commonly recognized heart attack sign in women. According to the american heart association, some women may even think their heart attack symptoms are flu-like symptoms. A heart attack can cause exhaustion due to the extra stress on your heart to try to pump while an area of blood flow is blocked. Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.
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Hello endocrinologist doctor, I am thalassemia major by birth my age is 26 yrs/m. But my voice and my look is childish like 12-15 years old boy. I want to treat my childish look and thin voice problem. I want to consult you online for its treatment but pls tell me if any tests to be done before for this problem so I can start the consultation without interruption in between. Pls.

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow of Academy of General Education (FAGE)
General Physician, Delhi
Hello endocrinologist doctor, I am thalassemia major by birth my age is 26 yrs/m. But my voice and my look is childis...
I am sorry to hear about your concern but will be happy to assist you. The vocal cords are smaller. The space inside there, where the vocal cords live, is all small, and the vocal cords are tiny. That's why it sounds thin and high. So, little kids sound like little kids because they have little cords. Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.
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This is for a marriage match. Both boy and girl are thalassemia carrier. Hb a2 value is 30.6 for boy and 34.1 for girl. Want to know about the perspective of having a baby in future. What precaution should be taken?

BHMS
Homeopathy Doctor, Hooghly
This is for a marriage match. Both boy and girl are thalassemia carrier. Hb a2 value is 30.6 for boy and 34.1 for gir...
Well now a days treatment is available which can be done during pregnancy, you need to consult with your gynaecologist for this purpose,
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Hi sir, if both partners are normal, they do not have thalassemia minor. Is there have a possibility that they may have a thalassemia minor baby?

MBBS, Basic Life Support (B.L.S), Advanced Cardiac Life Support, Fellow of Academy of General Education (FAGE)
General Physician, Delhi
Hi sir, if both partners are normal, they do not have thalassemia minor. Is there have a possibility that they may ha...
I am sorry to hear about your concern but will be happy to assist you. If both parents have beta thalassemia trait there is a 25 percent (1 in 4) chance with each pregnancy of having a child with beta thalassemia disease. Beta thalassemia disease is a lifelong illness that can result in serious health problems. These are the possible outcomes with each pregnancy. Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.
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