"Hemoglobin SC Disease" 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.
One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.
| Descriptor ID |
D006450
|
| MeSH Number(s) |
C15.378.071.141.150.150.440 C15.378.420.155.440 C16.320.070.150.440 C16.320.365.155.440
|
| Concept/Terms |
Hemoglobin SC Disease- Hemoglobin SC Disease
- Disease, Hemoglobin SC
- Diseases, Hemoglobin SC
- Hemoglobin SC Diseases
- SC Disease, Hemoglobin
- SC Diseases, Hemoglobin
- Sickle Cell Hemoglobin C Disease
- SC Disease
- Disease, SC
- Diseases, SC
- SC Diseases
|
Below are MeSH descriptors whose meaning is more general than "Hemoglobin SC Disease".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Anemia, Sickle Cell [C15.378.071.141.150.150]
- Hemoglobin SC Disease [C15.378.071.141.150.150.440]
- Hemoglobinopathies [C15.378.420]
- Anemia, Sickle Cell [C15.378.420.155]
- Hemoglobin SC Disease [C15.378.420.155.440]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Anemia, Sickle Cell [C16.320.070.150]
- Hemoglobin SC Disease [C16.320.070.150.440]
- Hemoglobinopathies [C16.320.365]
- Anemia, Sickle Cell [C16.320.365.155]
- Hemoglobin SC Disease [C16.320.365.155.440]
Below are MeSH descriptors whose meaning is more specific than "Hemoglobin SC Disease".
This graph shows the total number of publications written about "Hemoglobin SC Disease" by people in this website by year, and whether "Hemoglobin SC Disease" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 1998 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
Below are the most recent publications written about "Hemoglobin SC Disease" by people in Profiles.
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Epidemiological and clinical features, therapeutic strategies and outcomes in patients with hyperhaemolysis: A systematic review. Br J Haematol. 2023 06; 201(6):1025-1032.
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Unusually High Prevalence of Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease: A Retrospective Single Institution Study. Acta Haematol. 2022; 145(2):160-169.
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Predicting changes in hemoglobin S after simple transfusion using complete blood counts. Transfusion. 2018 01; 58(1):138-144.
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Thromboelastographic characterization of the activated clotting system in children with sickle cell trait or sickle cell disease. Thromb Res. 2017 Mar; 151:44-50.
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Conjunctival microvascular haemodynamics in sickle cell retinopathy. Acta Ophthalmol. 2015 Jun; 93(4):e275-80.
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Keeping it in the family: three relatives with HbSC disease and simultaneous acute pulmonary emboli. Am J Hematol. 2012 Jan; 87(1):101-4.
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The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial. Br J Haematol. 2011 Mar; 152(6):771-6.
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Low dose, oral epsilon aminocaproic acid for renal papillary necrosis and massive hemorrhage in hemoglobin SC disease. Pediatr Blood Cancer. 2010 Jan; 54(1):148-50.
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Pantaloon hip spica cast and constrained liner for the treatment of early total hip dislocation in a young patient with sickle cell disease. Am J Orthop (Belle Mead NJ). 2009 Dec; 38(12):E184-6.
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Acute myocardial infarction in hemoglobin SC disease. Ann Hematol. 2004 Oct; 83(10):622-4.