Epidermodysplasia Verruciformis
"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 |
|---|
| 2014 | 1 | 0 | 1 |
| 2018 | 3 | 0 | 3 |
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 2 | 0 | 2 |
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Below are the most recent publications written about "Epidermodysplasia Verruciformis" by people in Profiles.
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Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review. Genet Med. 2024 02; 26(2):101028.
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Whole transcriptome-based skin virome profiling in typical epidermodysplasia verruciformis reveals a-, ?-, and ?-HPV infections. JCI Insight. 2023 03 08; 8(5).
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Condyloma and coincidental epidermodysplasia verruciformis acanthoma positive for human papillomavirus-14 and -21. J Cutan Pathol. 2023 Jan; 50(1):47-50.
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Eosinophilic homogeneous intracytoplasmic inclusion bodies: Unique viral cytopathic changes associated with epidermodysplasia verruciformis and human papillomavirus type 49. J Cutan Pathol. 2022 Jul; 49(7):658-662.
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Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes. J Invest Dermatol. 2022 05; 142(5):1265-1269.
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Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma. Clin Infect Dis. 2019 05 17; 68(11):1938-1941.
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A CIB1 Splice-Site Founder Mutation in Families with?Typical Epidermodysplasia Verruciformis. J Invest Dermatol. 2019 05; 139(5):1195-1198.
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The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to ?-papillomaviruses. J Exp Med. 2018 09 03; 215(9):2289-2310.
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Epidermodysplasia Verruciformis: Genetic Heterogeneity and EVER1 and EVER2 Mutations Revealed by Genome-Wide Analysis. J Invest Dermatol. 2019 01; 139(1):241-244.
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Compound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy. J Clin Immunol. 2014 Oct; 34(7):871-90.