 Vitamin E Deficiency
"Vitamin E Deficiency" 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 nutritional condition produced by a deficiency of VITAMIN E in the diet, characterized by posterior column and spinocerebellar tract abnormalities, areflexia, ophthalmoplegia, and disturbances of gait, proprioception, and vibration. In premature infants vitamin E deficiency is associated with hemolytic anemia, thrombocytosis, edema, intraventricular hemorrhage, and increasing risk of retrolental fibroplasia and bronchopulmonary dysplasia. An apparent inborn error of vitamin E metabolism, named familial isolated vitamin E deficiency, has recently been identified. (Cecil Textbook of Medicine, 19th ed, p1181)
| Descriptor ID |
D014811
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| MeSH Number(s) |
C18.654.521.500.133.841
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| Concept/Terms |
Vitamin E Deficiency- Vitamin E Deficiency
- Deficiency, Vitamin E
- Deficiencies, Vitamin E
- Vitamin E Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Vitamin E Deficiency".
Below are MeSH descriptors whose meaning is more specific than "Vitamin E Deficiency".
This graph shows the total number of publications written about "Vitamin E Deficiency" by people in this website by year, and whether "Vitamin E Deficiency" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 | | 2002 | 0 | 1 | 1 |
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Below are the most recent publications written about "Vitamin E Deficiency" by people in Profiles.
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Maulik G, Salgia R, Makrigiorgos GM. Flow cytometric determination of lipid peroxidation using fluoresceinated phosphoethanolamine. Methods Enzymol. 2002; 352:80-91.
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Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T. Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency. Ann Neurol. 1996 Mar; 39(3):295-300.
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Huttenlocher PR, Gilles FH. Infantile neuroaxonal dystrophy. Clinical, pathologic, and histochemical findings in a family with 3 affected siblings. Neurology. 1967 Dec; 17(12):1174-84.
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