"Epidermodysplasia Verruciformis" 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 autosomal recessive trait with impaired cell-mediated immunity. About 15 human papillomaviruses are implicated in associated infection, four of which lead to skin neoplasms. The disease begins in childhood with red papules and later spreads over the body as gray or yellow scales.
| Descriptor ID |
D004819
|
| MeSH Number(s) |
C02.256.650.810.345 C02.825.810.260 C02.928.914.345 C17.800.838.790.810.260
|
| Concept/Terms |
Epidermodysplasia Verruciformis- Epidermodysplasia Verruciformis
- Lewandowsky-Lutz Disease
- Disease, Lewandowsky-Lutz
- Lewandowsky Lutz Disease
- Lutz-Lewandowsky Disease
- Disease, Lutz-Lewandowsky
- Lutz Lewandowsky Disease
|
Below are MeSH descriptors whose meaning is more general than "Epidermodysplasia Verruciformis".
Below are MeSH descriptors whose meaning is more specific than "Epidermodysplasia Verruciformis".
This graph shows the total number of publications written about "Epidermodysplasia Verruciformis" by people in this website by year, and whether "Epidermodysplasia Verruciformis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Epidermodysplasia Verruciformis" by people in Profiles.
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A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family. Clin Exp Dermatol. 2023 03 22; 48(4):434-437.
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Gene expression is stable in a complete CIB1 knockout keratinocyte model. Sci Rep. 2020 09 11; 10(1):14952.
MeSH information
