"Hyperkeratosis, Epidermolytic" 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 form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by ERYTHRODERMA and severe hyperkeratosis. It is manifested at birth by blisters followed by the appearance of thickened, horny, verruciform scales over the entire body, but accentuated in flexural areas. Mutations in the genes that encode KERATIN-1 and KERATIN-10 have been associated with this disorder.
| Descriptor ID |
D017488
|
| MeSH Number(s) |
C16.131.831.512.400.375 C16.320.850.400.375 C16.614.492.400.375 C17.800.428.333.250.375 C17.800.804.512.400.375 C17.800.827.400.375
|
| Concept/Terms |
Hyperkeratosis, Epidermolytic- Hyperkeratosis, Epidermolytic
- Epidermolytic Hyperkeratoses
- Hyperkeratoses, Epidermolytic
- Bullous Congenital Ichthyosiform Erythroderma
- Congenital Bullous Ichthyosiform Erythroderma
- Ichthyosiform Erythroderma, Bullous Congenital
- Epidermolytic Ichthyosis
- Bullous Ichthyosiform Erythroderma Congenital
- Bullous Erythroderma Ichthyosiformis Congenita of Brocq
- Bullous Ichthyosiform Erythroderma
- Bullous Ichthyosiform Erythrodermas
- Erythroderma, Bullous Ichthyosiform
- Erythrodermas, Bullous Ichthyosiform
- Ichthyosiform Erythroderma, Bullous
- Ichthyosiform Erythrodermas, Bullous
- Epidermolytic Hyperkeratosis
- Bullous Erythroderma Ichthyosiforme
- Erythroderma Ichthyosiforme, Bullous
- Bullous Erythroderma Ichthyosiformes
- Erythroderma Ichthyosiformes, Bullous
- Ichthyosiforme, Bullous Erythroderma
- Ichthyosiformes, Bullous Erythroderma
- Congenital Ichthyosiform Erythroderma, Bullous
|
Below are MeSH descriptors whose meaning is more general than "Hyperkeratosis, Epidermolytic".
- Diseases [C]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Skin Abnormalities [C16.131.831]
- Ichthyosis [C16.131.831.512]
- Ichthyosiform Erythroderma, Congenital [C16.131.831.512.400]
- Hyperkeratosis, Epidermolytic [C16.131.831.512.400.375]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
- Hyperkeratosis, Epidermolytic [C16.320.850.400.375]
- Infant, Newborn, Diseases [C16.614]
- Ichthyosis [C16.614.492]
- Ichthyosiform Erythroderma, Congenital [C16.614.492.400]
- Hyperkeratosis, Epidermolytic [C16.614.492.400.375]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Keratosis [C17.800.428]
- Ichthyosis [C17.800.428.333]
- Ichthyosiform Erythroderma, Congenital [C17.800.428.333.250]
- Hyperkeratosis, Epidermolytic [C17.800.428.333.250.375]
- Skin Abnormalities [C17.800.804]
- Ichthyosis [C17.800.804.512]
- Ichthyosiform Erythroderma, Congenital [C17.800.804.512.400]
- Hyperkeratosis, Epidermolytic [C17.800.804.512.400.375]
- Skin Diseases, Genetic [C17.800.827]
- Ichthyosiform Erythroderma, Congenital [C17.800.827.400]
- Hyperkeratosis, Epidermolytic [C17.800.827.400.375]
Below are MeSH descriptors whose meaning is more specific than "Hyperkeratosis, Epidermolytic".
This graph shows the total number of publications written about "Hyperkeratosis, Epidermolytic" by people in this website by year, and whether "Hyperkeratosis, Epidermolytic" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hyperkeratosis, Epidermolytic" by people in Profiles.
-
Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. Acta Derm Venereol. 2016 May; 96(4):473-8.
MeSH information
