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Aplastic Anemia

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Understanding the Rare Blood Disorder

Aplastic anemia is a rare and serious blood disorder that affects the bone marrow’s ability to produce enough new blood cells. It is characterized by a decrease in the number of red blood cells, white blood cells, and platelets in the body. This condition can lead to fatigue, increased susceptibility to infections, and uncontrolled bleeding. We are Leading Aplastic Anemia treatment center in Pune.

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There are two main types of thalassemia: alpha thalassemia and beta thalassemia. Each type has different subtypes, which can vary in severity.

1.Alpha Thalassemia: This type occurs when there is a problem with the production of alpha globin chains, a component of hemoglobin. The severity of alpha thalassemia depends on the number of affected genes. Subtypes include silent carrier, alpha thalassemia trait, hemoglobin H disease, and hydrops fetalis.

2.Beta Thalassemia: Beta thalassemia occurs when there is a mutation or absence of the beta globin chains. The severity of beta thalassemia can range from mild to severe. Subtypes include thalassemia minor, thalassemia intermedia, and thalassemia major (also known as Cooley’s anemia).

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Thalassemia is caused by mutations in the genes responsible for producing hemoglobin. These mutations can be inherited from one or both parents. If both parents carry thalassemia genes, their child has a higher chance of inheriting a more severe form of the disorder.

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The symptoms of thalassemia can vary depending on the type and severity of the condition bone marrow transplant treament. Common symptoms include:

  • Fatigue and weakness
  • Pale or yellowish skin
  • Delayed growth and development in children
  • Bone deformities and skeletal abnormalities
  • Enlarged spleen and liver
  • Shortness of breath
  • Jaundice

It is important to note that symptoms may not be present in individuals with mild forms of thalassemia. You will get best treatment for sickle cell anemia by Dr. Liza Bulsara

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Thalassemia can be diagnosed through various tests, including:

1.Complete Blood Count (CBC): This test measures the number of red blood cells, white blood cells, and platelets in the blood. Abnormalities in these counts can indicate thalassemia.

2.Hemoglobin Electrophoresis: This test identifies the different types of hemoglobin present in the blood, helping to determine the specific type of thalassemia.

3.Genetic Testing: Genetic testing can confirm the presence of thalassemia genes and determine the likelihood of passing them on to future generations.

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The treatment of thalassemia depends on the type and severity of the condition. Our Comprehensive Thalassemia Treatment Center and care to our patient.  Common treatment options include:

Care of thalassemic patient :

1.Blood Transfusions: Regular blood transfusions can help replace the deficient or abnormal red blood cells with healthy ones, improving oxygen delivery.

2.Iron Chelation Therapy: Due to the frequent blood transfusions, individuals with thalassemia may accumulate excess iron in their bodies. Iron chelation therapy helps remove the excess iron to prevent organ damage.

Cure of thalassemic patient :

  1. Stem Cell Transplantation: In severe cases, a stem cell transplant, also known as a bone marrow transplant, may be considered. This procedure involves replacing the faulty stem cells with healthy ones to restore normal blood cell production.
  2. Supportive Care: Managing symptoms and complications associated with thalassemia, such as infections, bone deformities, and organ damage, requires ongoing medical care and support
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