Elliptocytosis, Hereditary
"Elliptocytosis, 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.
An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
MeSH Number(s)
C15.378.071.141.150.365
C16.320.070.365
Concept/Terms
Elliptocytosis, Hereditary- Elliptocytosis, Hereditary
- Elliptocytoses, Hereditary
- Hereditary Elliptocytoses
- Hereditary Elliptocytosis
- Ovalocytosis, Hereditary
- Hereditary Ovalocytoses
- Hereditary Ovalocytosis
- Ovalocytoses, Hereditary
Below are MeSH descriptors whose meaning is more general than "Elliptocytosis, 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]
- Elliptocytosis, Hereditary [C15.378.071.141.150.365]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Elliptocytosis, Hereditary [C16.320.070.365]
Below are MeSH descriptors whose meaning is more specific than "Elliptocytosis, Hereditary".
This graph shows the total number of publications written about "Elliptocytosis, Hereditary" by people in Harvard Catalyst Profiles by year, and whether "Elliptocytosis, Hereditary" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1993 | 0 | 1 | 1 |
| 1994 | 1 | 0 | 1 |
| 1995 | 1 | 0 | 1 |
| 1998 | 2 | 0 | 2 |
| 2001 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2020 | 0 | 1 | 1 |
Below are the most recent publications written about "Elliptocytosis, Hereditary" by people in Profiles.
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Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia. J Clin Endocrinol Metab. 2020 12 01; 105(12).
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Accurate light microscopic diagnosis of South-East Asian ovalocytosis. Int J Lab Hematol. 2018 Dec; 40(6):655-662.
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Can exchange transfusions using red blood cells from donors with Southeast Asian ovalocytosis prevent or ameliorate cerebral malaria in patients with multi-drug resistant Plasmodium falciparum? Transfus Apher Sci. 2017 Dec; 56(6):865-866.
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X-linked elliptocytosis with impaired growth is related to mutated AMMECR1. Gene. 2017 Mar 30; 606:47-52.
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Membrane compartmentalization in Southeast Asian ovalocytosis red blood cells. Br J Haematol. 2011 Oct; 155(1):111-21.
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Flow cytometric osmotic fragility--an effective screening approach for red cell membranopathies. Cytometry B Clin Cytom. 2011 May; 80(3):186-90.
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Molecular physiology of SLC4 anion exchangers. Exp Physiol. 2006 Jan; 91(1):153-61.
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Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis. Blood. 2001 Jan 15; 97(2):543-50.
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Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome? J Med Genet. 1998 Apr; 35(4):273-8.
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FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation. Genomics. 1998 Feb 01; 47(3):350-8.