"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 1 | 1 | 2 |
| 2006 | 1 | 0 | 1 |
| 2007 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hemoglobin SC Disease" by people in Profiles.
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Essential thrombocythemia complicating hemoglobin SC disease and presenting with priapism. Blood. 2022 04 07; 139(14):2258.
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Original Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease. Exp Biol Med (Maywood). 2016 04; 241(7):737-44.
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Hydroxyurea treatment of children with hemoglobin SC disease. Pediatr Blood Cancer. 2013 Feb; 60(2):323-5.
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Recurrent intrahepatic pigmented stones after liver transplantation in a patient with hemoglobin SC disease: case report and review of the literature. Pediatr Transplant. 2011 Aug; 15(5):519-24.
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Acute splenic sequestration in an adult with hemoglobin S-C disease. Am J Emerg Med. 2008 Nov; 26(9):1064.e5-8.
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Staged single-ventricle palliation in an infant with hemoglobin SC disease. Tex Heart Inst J. 2007; 34(4):439-41.
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Limb amputation in hemoglobin SC disease after application of ice and elevation. Am J Hematol. 2007 Jan; 82(1):53-4.
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Successful mobilization and transplantation of filgrastim mobilized hematopoietic stem cells in sickle cell-hemoglobin C disease. Bone Marrow Transplant. 2006 Jun; 37(11):1065-6.
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Transient left ventricular dysfunction in childhood sickle cell disease. Pediatr Cardiol. 1999 May-Jun; 20(3):221-3.
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Successful hydroxyurea treatment of a patient with SD hemoglobinopathy. Am J Hematol. 1999 Jan; 60(1):84-5.