Examples of 'beta thalassemia' in a sentence
Meaning of "beta thalassemia"
beta thalassemia - Beta thalassemia is a genetic blood disorder characterized by reduced or absent production of hemoglobin, leading to anemia and other complications. It is caused by mutations in the beta-globin gene and can range from mild to severe forms, requiring monitoring, treatment, and management by healthcare professionals
How to use "beta thalassemia" in a sentence
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beta thalassemia
Beta thalassemia is a hereditary disease affecting hemoglobin.
Zoe is a carrier for beta thalassemia.
Beta thalassemia is caused by mutations in these genes.
The levels can be normal to increased in beta thalassemia.
Beta thalassemia may also result in transfusion dependence.
This person is termed as heterozygous for beta thalassemia.
Beta thalassemia patient builds app to help manage anaemia.
Other families who have a child with beta thalassemia.
Individuals with beta thalassemia major require regular blood transfusions.
The picture shows one example of how beta thalassemia is inherited.
Kids with beta thalassemia trait usually do not need treatment.
And the baby tested positive for the beta thalassemia trait.
Beta thalassemia is caused by mutations in one or both of the beta globin genes.
Family history and ancestry are factors which increase the risk of beta thalassemia.
People who have beta thalassemia intermedia have mild to moderate anemia.
See also
One is for sickle cell disease and another is a similar genetic condition called beta thalassemia.
People with beta thalassemia are at an increased risk of developing abnormal blood clots.
Mutation in this gene is responsible for beta thalassemia and sickle cell anemia.
People with beta thalassemia trait will have lifelong mild anemia.
Blood transfusions may be needed occasionally should you have beta thalassemia intermedia or hemoglobin H disease.
Beta thalassemia minor occurs when only one of the beta chains is defected.
The only known cure for Beta Thalassemia Major is a stem cell transplant.
Beta thalassemia is a hereditary disease allowing for a preventative treatment by carrier screening and prenatal diagnosis.
In some embodiments, the disease or disorder is beta thalassemia.
People with beta thalassemia major may need regular blood transfusions every four to six weeks.
There are two main types, alpha thalassemia and beta thalassemia.
Beta Thalassemia is due to the decreased production of beta globin.
As an inherited disorder, beta thalassemia can only be passed on genetically.
For example, my sister has a condition called beta thalassemia minor.
Patients with Beta Thalassemia have severe anemia.
Results, and the baby tested positive for the beta thalassemia trait.
She had beta thalassemia minor, so age is not a factor.
For example, two variants that are elevated in beta thalassemia are HbF and HbA2.
Less severe forms of beta thalassemia usually do not shorten the person 's lifespan.
Future treatments-Researchers are working to find possible new treatments for beta thalassemia.
In beta thalassemia major, regular blood transfusions are required, sometimes every few weeks.
And the baby tested positive for the beta thalassemia trait. That's just a marker.
Beta thalassemia major, an inherited form of anemia, is treated with monthly blood transfusions.
The method of embodiment 74, wherein the disease or disorder is beta thalassemia.
Children and adults with beta thalassemia major need lifelong medical care that includes,.
OTL-300 was being tested in the trial as a treatment for transfusion dependent beta thalassemia.
This test can diagnose beta thalassemia and other hemoglobin changes, but not alpha thalassemia.
In the United States, the FDA approved clinical trials on Beta thalassemia patients in 2012.
Beta thalassemia major is also known as Cooley 's anemia.
And the baby tested positive for the beta thalassemia trait. S. Results.
Both alpha and beta thalassemia include the following 2 forms, Thalassemia major and Thalassemia minor.
Treatment for beta thalassemia major or Cooley 's anemia.
Beta thalassemia ( β thalassemia ) occurs if one or both genes are altered.
Treatments for Beta thalassemia major ( Beta thalassemia ) include,.
Beta thalassemia is caused by mutations in the HBB gene on chromosome 11.
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Beta thalassemia is a hereditary disease affecting hemoglobin
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