 Hemoglobin SC Disease
"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
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| 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
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| 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
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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 |
|---|
| 1994 | 0 | 1 | 1 | | 1995 | 1 | 0 | 1 | | 1998 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2023 | 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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D'Alessandro A, Nouraie SM, Zhang Y, Cendali F, Gamboni F, Reisz JA, Zhang X, Bartsch KW, Galbraith MD, Espinosa JM, Gordeuk VR, Gladwin MT. Metabolic signatures of cardiorenal dysfunction in plasma from sickle cell patients as a function of therapeutic transfusion and hydroxyurea treatment. Haematologica. 2023 12 01; 108(12):3418-3432.
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Kammeyer R, Devnani R, Mehta R. Cerebral fat embolism syndrome mimicking thrombotic thrombocytopenic purpura in a patient with hemoglobin SC disease. Am J Hematol. 2016 May; 91(5):539-42.
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McKinney CM, Siringo F, Olson JL, Capocelli KE, Ambruso DR, Nuss R. Red cell exchange transfusion halts progressive proliferative sickle cell retinopathy in a teenaged patient with hemoglobin SC disease. Pediatr Blood Cancer. 2015 Apr; 62(4):721-3.
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Micel L, Nuss R, Fenton L, Lovell M, Silliman CC. Non-palpable splenic enlargement as the etiology of abdominal pain in an adolescent with hemoglobin SC disease. Pediatr Blood Cancer. 2011 Aug; 57(2):352-3.
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Wang-Gillam A, Lee RS, Hsi ED, Brotman DJ. Acute splenic sequestration crisis resembling sepsis in an adult with hemoglobin SC disease. South Med J. 2004 Apr; 97(4):413-5.
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Neumayr L, Koshy M, Haberkern C, Earles AN, Bellevue R, Hassell K, Miller S, Black D, Vichinsky E. Surgery in patients with hemoglobin SC disease. Preoperative Transfusion in Sickle Cell Disease Study Group. Am J Hematol. 1998 Feb; 57(2):101-8.
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Lane PA, O'Connell JL, Lear JL, Rogers ZR, Woods GM, Hassell KL, Wethers DL, Luckey DW, Buchanan GR. Functional asplenia in hemoglobin SC disease. Blood. 1995 Apr 15; 85(8):2238-44.
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Hassell KL, Eckman JR, Lane PA. Acute multiorgan failure syndrome: a potentially catastrophic complication of severe sickle cell pain episodes. Am J Med. 1994 Feb; 96(2):155-62.
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Wilimas JA, Flynn PM, Harris S, Day SW, Smith R, Chesney PJ, Rodman JH, Eguiguren JM, Fairclough DL, Wang WC. A randomized study of outpatient treatment with ceftriaxone for selected febrile children with sickle cell disease. N Engl J Med. 1993 Aug 12; 329(7):472-6.
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Broxson EH, Sokol RJ, Githens JH. Normal vitamin E status in sickle hemoglobinopathies in Colorado. Am J Clin Nutr. 1989 Sep; 50(3):497-503.
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