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Science City Road, Sola, Ahmedabad

Thalassemia Treatment in Ahmedabad

Hematology · Thalassemia

Specialist for Thalassemia Treatment in Ahmedabad

Dr. Aishwarya Raj provides consultation and treatment for Thalassemia, with a focus on compassionate care. With a deep understanding of the condition and a patient-centric approach, She provides evidence-based treatment, helping patients manage the condition.

  • Experienced specialist care in Thalassemia treatment.
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Thalassemia
Overview

What is Thalassemia?

Thalassemia is a genetic blood disorder that affects the production of hemoglobin, the protein responsible for carrying oxygen in red blood cells. It is characterized by abnormal or insufficient production of one or more globin chains that make up hemoglobin. Thalassemia is typically inherited from parents who carry the mutated genes.

Diagnosis of thalassemia involves blood tests, including a complete blood count and hemoglobin electrophoresis, which can help identify abnormal hemoglobin patterns. Genetic testing may also be performed to determine the specific genetic mutations involved.

Treatment options for thalassemia vary depending on the severity and symptoms of the condition. They may include regular blood transfusions to increase hemoglobin levels, iron chelation therapy to remove excess iron from the body, and folic acid supplements to support red blood cell production. In some cases, bone marrow or stem cell transplantation may be considered as a curative option.

Symptoms

Symptoms :

Tap the symptoms you have noticed.

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Causes

Causes of Thalassemia :

  1. 01

    Alpha thalassemia

  2. 02

    Beta thalassemia

Diagnosis

Diagnosis Test :

  1. 01

    Blood tests

  2. 02

    Hemoglobin electrophoresis

  3. 03

    Genetic testing

  4. 04

    Prenatal testing

Treatment

Treatment

  1. Blood transfusions
  2. Iron chelation therapy
  3. Folic acid supplementation
  4. Splenectomy
  5. Bone marrow transplantation
Your doctor

Specialist For Thalassemia Treatment

Dr. Aishwarya Raj

Dr. Aishwarya Raj

Hematologist
MBBS , MD , Fellowship in Clinical Hemato-Oncology

Dr. Aishwarya Raj (M.B.B.S., M.D., Fellowship in Hemato-Oncology) is the consultant hematologist at Aaryaa Endocrine Clinic and provides Thalassemia treatment. Dr. Raj focuses on careful evaluation and individualised, evidence-based care.

With years of experience and extensive knowledge in Thalassemia, Dr. Raj offers comprehensive and personalized treatment plans for patients. She understands the complexities of Thalassemia and recognizes the importance of tailoring treatment to meet the unique needs of each individual.

Dr. Raj stays up-to-date with the latest advancements in Thalassemia research and treatment modalities. Her approach combines evidence-based practices with compassionate care, with attention to each patient's individual needs.

For Thalassemia treatment, you can consult Dr. Raj at Aaryaa Endocrine Clinic. Take the first step towards effective Thalassemia management and a healthier life.

FAQs

Frequently Asked Questions

Have another question about Thalassemia treatment? Call or message the clinic.

Call +91 93161 33482

Thalassemia is a genetic blood disorder characterized by abnormal or insufficient production of hemoglobin, the protein responsible for carrying oxygen in red blood cells. It is caused by mutations in the genes that control the production of globin chains, leading to an imbalance in the production of these chains and abnormal red blood cell formation.

There are two main types of thalassemia: alpha thalassemia and beta thalassemia. Alpha thalassemia occurs when there are defects in the genes responsible for alpha globin chain production, while beta thalassemia occurs when there are defects in the genes responsible for beta globin chain production.

Thalassemia is usually inherited in an autosomal recessive manner, which means that both parents must carry and pass on the mutated genes for their child to have thalassemia. If both parents are carriers, each child has a 25% chance of having thalassemia, a 50% chance of being a carrier like their parents, and a 25% chance of neither having thalassemia nor being a carrier.