Spherocytosis, Hereditary
"Spherocytosis, Hereditary" 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 group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
| Descriptor ID |
D013103
|
| MeSH Number(s) |
C15.378.071.141.150.785 C16.320.070.785
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Spherocytosis, Hereditary".
- 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]
- Spherocytosis, Hereditary [C15.378.071.141.150.785]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Spherocytosis, Hereditary [C16.320.070.785]
Below are MeSH descriptors whose meaning is more specific than "Spherocytosis, Hereditary".
This graph shows the total number of publications written about "Spherocytosis, Hereditary" by people in this website by year, and whether "Spherocytosis, Hereditary" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Spherocytosis, Hereditary" by people in Profiles.
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A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome. Intern Med. 2023 Jan 01; 62(1):107-111.
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Clinical and laboratory outcomes following total or partial splenectomy in patients with hereditary spherocytosis. Pediatr Hematol Oncol. 2019 Sep; 36(6):382-389.
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Orthotopic heart transplantation in a child with hereditary spherocytosis. Artif Organs. 2010 Dec; 34(12):1154-6.
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Laparoscopic splenectomy in children. JSLS. 2005 Oct-Dec; 9(4):389-92.
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Clinical presentation of parvovirus B19 infection in children with aplastic crisis. Pediatr Infect Dis J. 2003 Dec; 22(12):1100-1.
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Hemolysis and deformability of erythrocytes exposed to butoxyacetic acid, a metabolite of 2-butoxyethanol: II. Resistance in red blood cells from humans with potential susceptibility. J Appl Toxicol. 1994 Mar-Apr; 14(2):97-102.
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Splenic sequestration associated with sickle cell trait and hereditary spherocytosis. Am J Hematol. 1992 Jun; 40(2):110-6.
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Effect of splenectomy of hepatic bilirubin clearance in patients with hereditary spherocytosis. Implications for the diagnosis of Gilbert's syndrome. J Lab Clin Med. 1981 Jul; 98(1):37-45.
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Transient erythroid aplasia in hemolytic anemia: a review of the literature with two case reports. Tex Rep Biol Med. 1974; 32(2):391-411.