"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 |
|---|
| 2005 | 0 | 1 | 1 |
| 2008 | 0 | 2 | 2 |
| 2010 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2016 | 2 | 0 | 2 |
| 2020 | 1 | 0 | 1 |
| 2022 | 2 | 0 | 2 |
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Below are the most recent publications written about "Keratoderma, Palmoplantar" by people in Profiles.
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A new de novo heterozygous missense mutation in the desmoplakin gene, causing Naxos and Carvajal disease, associating oligodontia and nail fragility. Clin Exp Dermatol. 2022 Jul; 47(7):1424-1426.
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Cole disease due to a novel pathogenic variant in the ENPP1 gene. J Eur Acad Dermatol Venereol. 2022 07; 36(7):e559-e561.
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Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndrome. Br J Dermatol. 2020 10; 183(4):756-757.
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Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome. J Inherit Metab Dis. 2017 05; 40(3):461-462.
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Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability. Acta Derm Venereol. 2016 May; 96(4):468-72.
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Nonsense mutations in AAGAB cause punctate palmoplantar keratoderma type Buschke-Fischer-Brauer. Am J Hum Genet. 2012 Oct 05; 91(4):754-9.
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Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene. Eur J Med Genet. 2011 May-Jun; 54(3):205-8.
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Identification of two new mutations in the TAT gene in a Danish family with tyrosinaemia type II. Br J Dermatol. 2009 Mar; 160(3):704-6.
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Richner-Hanhart syndrome detected by expanded newborn screening. Pediatr Dermatol. 2008 May-Jun; 25(3):378-80.
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Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triad. Eur J Dermatol. 2005 Sep-Oct; 15(5):347-52.
MeSH information
