What does beta thalassemia mean?
Definitions for beta thalassemia
be·ta tha·lassemi·a
This dictionary definitions page includes all the possible meanings, example usage and translations of the word beta thalassemia.
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Wikipedia
Beta thalassemia
Beta thalassemias (β thalassemias) are a group of inherited blood disorders. They are forms of thalassemia caused by reduced or absent synthesis of the beta chains of hemoglobin that result in variable outcomes ranging from severe anemia to clinically asymptomatic individuals. Global annual incidence is estimated at one in 100,000. Beta thalassemias occur due to malfunctions in the hemoglobin subunit beta or HBB. The severity of the disease depends on the nature of the mutation.HBB blockage over time leads to decreased beta-chain synthesis. The body's inability to construct new beta-chains leads to the underproduction of HbA (adult hemoglobin). Reductions in HbA available overall to fill the red blood cells in turn leads to microcytic anemia. Microcytic anemia ultimately develops in respect to inadequate HBB protein for sufficient red blood cell functioning. Due to this factor, the patient may require blood transfusions to make up for the blockage in the beta-chains. Repeated blood transfusions cause severe problems associated with iron overload.
Numerology
Chaldean Numerology
The numerical value of beta thalassemia in Chaldean Numerology is: 7
Pythagorean Numerology
The numerical value of beta thalassemia in Pythagorean Numerology is: 1
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"beta thalassemia." Definitions.net. STANDS4 LLC, 2024. Web. 7 May 2024. <https://www.definitions.net/definition/beta+thalassemia>.
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