Keratoderma, Palmoplantar
"Keratoderma, Palmoplantar" 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.
Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis).
| Descriptor ID |
D007645
|
| MeSH Number(s) |
C16.320.850.475 C17.800.428.435 C17.800.827.475
|
| Concept/Terms |
Keratoderma, Palmoplantar- Keratoderma, Palmoplantar
- Keratodermas, Palmoplantar
- Palmoplantar Keratodermas
- Keratosis Palmaris et Plantaris
- Palmoplantar Keratoderma
- Hyperkeratosis Palmaris et Plantaris
- Keratosis, Palmoplantar
- Keratoses, Palmoplantar
- Palmoplantar Keratoses
- Palmoplantar Keratosis
Meleda Disease- Meleda Disease
- Disease, Meleda
- Keratosis Palmoplantaris Transgradiens of Siemens
- Mal de Meleda
- Meleda, Mal de
- de Meleda, Mal
|
Below are MeSH descriptors whose meaning is more general than "Keratoderma, Palmoplantar".
Below are MeSH descriptors whose meaning is more specific than "Keratoderma, Palmoplantar".
This graph shows the total number of publications written about "Keratoderma, Palmoplantar" by people in this website by year, and whether "Keratoderma, Palmoplantar" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Keratoderma, Palmoplantar" by people in Profiles.
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Bedoukian EC, Rentas S, Skraban C, Shao Q, Treat J, Laird DW, Sullivan KE. Palmoplantar keratoderma with deafness phenotypic variability in a patient with an inherited GJB2 frameshift variant and novel missense variant. Mol Genet Genomic Med. 2021 02; 9(2):e1574.