"Ichthyosiform Erythroderma, Congenital" 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.
Designation for several severe forms of ichthyosis, present at birth, that are characterized by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalized scaling. The forms include bullous (HYPERKERATOSIS, EPIDERMOLYTIC), non-bullous (ICHTHYOSIS, LAMELLAR), wet type, and dry type.
| Descriptor ID |
D016113
|
| MeSH Number(s) |
C16.131.831.512.400 C16.320.850.400 C16.614.492.400 C17.800.428.333.250 C17.800.804.512.400 C17.800.827.400
|
| Concept/Terms |
Ichthyosiform Erythroderma, Congenital- Ichthyosiform Erythroderma, Congenital
- Erythroderma, Congenital Ichthyosiform
- Congenital Ichthyosiform Erythrodermas
- Erythrodermas, Congenital Ichthyosiform
- Ichthyosiform Erythrodermas, Congenital
- Congenital Ichthyosiform Erythroderma
|
Below are MeSH descriptors whose meaning is more general than "Ichthyosiform Erythroderma, Congenital".
- 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]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
- Infant, Newborn, Diseases [C16.614]
- Ichthyosis [C16.614.492]
- Ichthyosiform Erythroderma, Congenital [C16.614.492.400]
- 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]
- Skin Abnormalities [C17.800.804]
- Ichthyosis [C17.800.804.512]
- Ichthyosiform Erythroderma, Congenital [C17.800.804.512.400]
- Skin Diseases, Genetic [C17.800.827]
- Ichthyosiform Erythroderma, Congenital [C17.800.827.400]
Below are MeSH descriptors whose meaning is more specific than "Ichthyosiform Erythroderma, Congenital".
This graph shows the total number of publications written about "Ichthyosiform Erythroderma, Congenital" by people in this website by year, and whether "Ichthyosiform Erythroderma, Congenital" 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 |
|---|
| 2021 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Ichthyosiform Erythroderma, Congenital" by people in Profiles.
-
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes (Basel). 2023 03 15; 14(3).
-
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients. Genes (Basel). 2021 01 09; 12(1).
MeSH information
