Beta thalassemia: Introduction
Beta thalassemia: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called alpha and beta. Beta thalassemia involves defects in one or more of the two genes required to make each ? protein chain. The main symptom is anemia, the severity of which can vary amongst patients depending on how many defective genes are involved.
More detailed information about the symptoms,
causes, and treatments of Beta thalassemia is available below.
Symptoms of Beta thalassemia
See full list of 18
symptoms of Beta thalassemia
Treatments for Beta thalassemia
- Mild cases may require no treatment. Regular blood transfusions are required in more severe cases. Removal (chelation) of iron buildup in body due to blood transfusion, folic acid supplements, surgical removal of spleen or allogeneic hematopoietic transplant may be helpful in some cases. Genetic counseling is recommended
- Blood transfusions, removal (chelation) of iron buildup in body due to blood transfusion, folic acid supplements, surgical removal of spleen or stem cell transplant. Genetic counseling is recommended
- Treatment of beta thalassemia depends on whether the patient is heterozygous (thalassemia minor) or Homozygous (thalassemia major) Treatments include:
- No treatment - for those with thalassemia minor
- Blood transfusion - lifelong for those with the severe homozygous form
- more treatments...»
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Home Diagnostic Testing
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Wrongly Diagnosed with Beta thalassemia?
Beta thalassemia: Related Patient Stories
Beta thalassemia: Deaths
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Beta thalassemia: Complications
Review possible medical complications related to Beta thalassemia:
Causes of Beta thalassemia
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Disease Topics Related To Beta thalassemia
Research the causes of these diseases that are similar to, or related to, Beta thalassemia:
Beta thalassemia: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Beta thalassemia
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Read more about Misdiagnosis and Beta thalassemia
Beta thalassemia: Research Doctors & Specialists
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Evidence Based Medicine Research for Beta thalassemia
Medical research articles related to Beta thalassemia include:
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Beta thalassemia: Animations
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Prognosis for Beta thalassemia
Prognosis for Beta thalassemia:
The prognosis varies depending on how severe the condition is but even the most severe form can result in a reasonable prognosis if treatment is delivered and complications are managed appropriately.
More about prognosis of Beta thalassemia
Research about Beta thalassemia
Visit our research pages for current research about Beta thalassemia treatments.
Clinical Trials for Beta thalassemia
The US based website ClinicalTrials.gov lists information on both federally
and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Beta thalassemia include:
See full list of 26
Clinical Trials for Beta thalassemia
Statistics for Beta thalassemia
Beta thalassemia: Broader Related Topics
Types of Beta thalassemia
User Interactive Forums
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Definitions of Beta thalassemia:
Beta thalassemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Beta thalassemia, or a subtype of Beta thalassemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Beta thalassemia as a "rare disease".
Source - Orphanet
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