Alpha thalassemia: Introduction
Alpha thalassemia: Thalassemia is an inherited blood disorder characterized by abnormal synthesis of hemoglobin. Hemoglobin consists of two main protein chains called alpha and beta. Alpha thalassemia involves defects in one or more of the four 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 Alpha thalassemia is available below.
Symptoms of Alpha thalassemia
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symptoms of Alpha thalassemia
Treatments for Alpha 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
- No treatment - for mild cases
- Folate supplementation as deficiency often occurs with high cell turnover
- Blood transfusion
- more treatments...»
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Home Diagnostic Testing
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Wrongly Diagnosed with Alpha thalassemia?
Alpha thalassemia: Deaths
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Alpha thalassemia: Complications
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Causes of Alpha thalassemia
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Disease Topics Related To Alpha thalassemia
Research the causes of these diseases that are similar to, or related to, Alpha thalassemia:
Alpha thalassemia: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Alpha thalassemia
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called Von Willebrand's disease is quite common in women, but often fails to be correctly diagnosed.
Women with the...read more »
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is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis)....read more »
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Alpha thalassemia: Research Doctors & Specialists
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Evidence Based Medicine Research for Alpha thalassemia
Medical research articles related to Alpha thalassemia include:
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Alpha thalassemia: Animations
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Prognosis for Alpha thalassemia
Prognosis for Alpha 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.
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Research about Alpha thalassemia
Visit our research pages for current research about Alpha thalassemia treatments.
Clinical Trials for Alpha 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 Alpha thalassemia include:
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Statistics for Alpha thalassemia
Alpha thalassemia: Broader Related Topics
Types of Alpha thalassemia
User Interactive Forums
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Definitions of Alpha thalassemia:
Alpha thalassemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Alpha thalassemia, or a subtype of Alpha 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 Alpha thalassemia as a "rare disease".
Source - Orphanet
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