"beta-Thalassemia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
| Descriptor ID |
D017086
|
| MeSH Number(s) |
C15.378.071.141.150.875.150 C15.378.420.826.150 C16.320.070.875.150 C16.320.365.826.150
|
| Concept/Terms |
beta-Thalassemia- beta-Thalassemia
- Microcytemia, beta Type
- Microcytemias, beta Type
- Type Microcytemia, beta
- Type Microcytemias, beta
- beta Type Microcytemia
- beta Type Microcytemias
- beta Thalassemia
- Thalassemia, beta
- Thalassemias, beta
- beta Thalassemias
- Thalassemia, beta Type
- Thalassemias, beta Type
- Type Thalassemia, beta
- Type Thalassemias, beta
- beta Type Thalassemia
- beta Type Thalassemias
Thalassemia Intermedia- Thalassemia Intermedia
- Intermedia, Thalassemia
- Intermedias, Thalassemia
- Thalassemia Intermedias
Thalassemia Minor- Thalassemia Minor
- Thalassemia Minor (beta-Thalassemia Minor)
- Minor, Thalassemia (beta-Thalassemia Minor)
- Minors, Thalassemia (beta-Thalassemia Minor)
- Thalassemia Minor (beta Thalassemia Minor)
- Thalassemia Minors (beta-Thalassemia Minor)
Thalassemia Major- Thalassemia Major
- Anemia, Erythroblastic
- Anemias, Erythroblastic
- Erythroblastic Anemia
- Thalassemia Major (beta-Thalassemia Major)
- Major, Thalassemia (beta-Thalassemia Major)
- Majors, Thalassemia (beta-Thalassemia Major)
- Thalassemia Major (beta Thalassemia Major)
- Thalassemia Majors (beta-Thalassemia Major)
- Mediterranean Anemia
- Anemias, Mediterranean
- Mediterranean Anemias
- Anemia, Cooley's
- Anemia, Cooley
- Anemia, Cooleys
- Cooley's Anemia
- Anemia, Mediterranean
|
Below are MeSH descriptors whose meaning is more general than "beta-Thalassemia".
Below are MeSH descriptors whose meaning is more specific than "beta-Thalassemia".
This graph shows the total number of publications written about "beta-Thalassemia" by people in this website by year, and whether "beta-Thalassemia" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "beta-Thalassemia" by people in Profiles.
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Efficacy and Safety of Combined Oral Chelation With Deferiprone and Deferasirox in Children With ß-Thalassemia Major: An Experience From North India. J Pediatr Hematol Oncol. 2017 04; 39(3):209-213.
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Health Related Quality of Life in Patients with Transfusion-dependent Thalassemia. Indian Pediatr. 2016 Aug 08; 53(8):741-2.
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Genomics of alternative splicing: evolution, development and pathophysiology. Hum Genet. 2014 Jun; 133(6):679-87.
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Cyclophosphamide-associated cardiotoxicity in a child after stem cell transplantation for ß-thalassemia major: case report and review of the literature. Pediatr Dev Pathol. 2014 Jan-Feb; 17(1):50-4.
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Red cell exchange is not effective for patients with sickle cell anaemia and coexisting warm autoantibody haemolysis. Blood Transfus. 2010 Oct; 8(4):303-6.
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A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. Hum Genet. 2010 Mar; 127(3):303-14.
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Preimplantation HLA typing with aneuploidy testing. Reprod Biomed Online. 2006 Jan; 12(1):89-100.
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Hemoglobin C disease. N Engl J Med. 2004 Oct 07; 351(15):1577; author reply 1577.
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Long-term efficacy of alpha-interferon in beta-thalassemics with chronic hepatitis C. Blood. 1997 Sep 15; 90(6):2207-12.
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Long-term assessment of efficacy and safety of L1, an oral iron chelator, in transfusion dependent thalassaemia: Indian trial. Br J Haematol. 1992 Oct; 82(2):460-6.