thalassemia

(redirected from Beta-thalassemia)
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Related to Beta-thalassemia: Alpha-thalassemia, Thalassemia minor
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Synonyms for thalassemia

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Naturally occurring increased levels of therapeutic fetal hemoglobin have been shown to reduce the severity of both SCD and beta-thalassemia disorders in adulthood.
2] peak is around 12%-16% on HPLC, Hb Lepore should be suspected since the maximum value of the HbA, fraction in beta-thalassemia trait is 8%-9%.
Beta-thalassemia trait prevalence in districts of Hatay was found as; Antakya 4.
Nutrient deficiencies are found in a large variety of anemias, while excessive iron is characteristic of beta-thalassemia major (Figure 1).
Polymerase chain reaction (PCR) mutagenesis enabling rapid non-radioactive detection of common beta-thalassemia mutations in Mediterraneans.
Alpha-thalassemia depresses only the production of the alpha chains, and beta-thalassemia depresses only the production of the beta chains.
ARDS in a patient with homozygous beta-thalassemia due to yersinosis.
Transferring a human gene into mouse stem cells alleviated the signs of a common inherited blood disorder called beta-thalassemia, according to a report in the July 6 issue of Nature.
Beta-thalassemia, a potentially life-threatening anemia, for instance, traces to inherited gene-splicing errors.
Scientists had discovered that beta-thalassemia resulted from gene flaws that disrupted the production of normal hemoglobin, the oxygen carrying pigment in blood.
This mechanism of action to increase red blood cells has the potential to treat patients with anemia in diseases such as myelodysplastic syndromes (MDS) and beta-thalassemia that are inadequately managed with current therapy.
One study shares follow-up data on patients who can forgo blood transfusion after receiving lentiviral gene therapy to treat beta-thalassemia.