"Skin Diseases, Papulosquamous" 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 dermatoses with distinct morphologic features. The primary lesion is most commonly a papule, usually erythematous, with a variable degree of scaling on the surface. Plaques form through the coalescing of primary lesions.
| Descriptor ID |
D017444
|
| MeSH Number(s) |
C17.800.859
|
| Concept/Terms |
Skin Diseases, Papulosquamous- Skin Diseases, Papulosquamous
- Papulosquamous Disorders
- Disorder, Papulosquamous
- Disorders, Papulosquamous
- Papulosquamous Disorder
- Papulosquamous Skin Diseases
- Disease, Papulosquamous Skin
- Diseases, Papulosquamous Skin
- Papulosquamous Skin Disease
- Skin Disease, Papulosquamous
|
Below are MeSH descriptors whose meaning is more general than "Skin Diseases, Papulosquamous".
Below are MeSH descriptors whose meaning is more specific than "Skin Diseases, Papulosquamous".
This graph shows the total number of publications written about "Skin Diseases, Papulosquamous" by people in this website by year, and whether "Skin Diseases, Papulosquamous" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 2 | 0 | 2 |
| 2017 | 2 | 1 | 3 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Skin Diseases, Papulosquamous" by people in Profiles.
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Mast cell activation in Dowling-Degos disease. Br J Dermatol. 2019 12; 181(6):1312-1314.
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Altered Notch Signaling in Dowling-Degos Disease: Additional Mutations in POGLUT1 and Further Insights into Disease Pathogenesis. J Invest Dermatol. 2019 04; 139(4):960-964.
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Functional implications of novel ADAM10 mutations in reticulate acropigmentation of Kitamura. Br J Dermatol. 2017 12; 177(6):e340-e343.
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Intra- and Interfamilial Phenotype Variability Associated with Mutations in ?-Secretase Subunit-Encoding PSENEN. J Invest Dermatol. 2018 05; 138(5):1215-1218.
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Mutations in ?-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa. J Clin Invest. 2017 Apr 03; 127(4):1485-1490.
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Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura. J Invest Dermatol. 2015 Feb; 135(2):615-618.
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Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease. Am J Hum Genet. 2014 Jan 02; 94(1):135-43.
MeSH information
