"Fetal Hemoglobin" 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.
The major component of hemoglobin in the fetus. This HEMOGLOBIN has two alpha and two gamma polypeptide subunits in comparison to normal adult hemoglobin, which has two alpha and two beta polypeptide subunits. Fetal hemoglobin concentrations can be elevated (usually above 0.5%) in children and adults affected by LEUKEMIA and several types of ANEMIA.
Descriptor ID |
D005319
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MeSH Number(s) |
D12.776.124.400.303 D12.776.422.316.762.320
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Fetal Hemoglobin".
Below are MeSH descriptors whose meaning is more specific than "Fetal Hemoglobin".
This graph shows the total number of publications written about "Fetal Hemoglobin" by people in this website by year, and whether "Fetal Hemoglobin" 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 |
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2013 | 0 | 1 | 1 |
2017 | 1 | 1 | 2 |
2018 | 2 | 0 | 2 |
2019 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fetal Hemoglobin" by people in Profiles.
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Simultaneous diagnosis of severe SARS-CoV-2 infection and sickle cell disease in two infants. Blood Transfus. 2021 03; 19(2):120-123.
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A hypothesis about the role of fetal hemoglobin in COVID-19. Med Hypotheses. 2020 Nov; 144:109994.
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COVID-19 in Newborns and Infants-Low Risk of Severe Disease: Silver Lining or Dark Cloud? Am J Perinatol. 2020 Jun; 37(8):845-849.
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Increased Prevalence of Thalassemia in Young People in Korea: Impact of Increasing Immigration. Ann Lab Med. 2019 Mar; 39(2):133-140.
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Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes. Ann Hematol. 2019 Apr; 98(4):833-840.
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Efficacy and safety of resveratrol, an oral hemoglobin F-augmenting agent, in patients with beta-thalassemia intermedia. Ann Hematol. 2018 Oct; 97(10):1919-1924.
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Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian Experience. Hemoglobin. 2017 Jul - Nov; 41(4-6):267-273.
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[Prenatal Diagnosis of A Case of SEA-HPFH Deletion Combined with Beta-Thalassemia in A Chinese Family]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Aug; 25(4):1142-1146.
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Multicenter evaluation of hemoglobin A1c assay on capillary electrophoresis. Clin Chim Acta. 2013 Sep 23; 424:207-11.