Ichthyosiform Erythroderma, Congenital
"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.
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 Harvard Catalyst Profiles by year, and whether "Ichthyosiform Erythroderma, Congenital" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
1999 | 1 | 0 | 1 |
2004 | 1 | 0 | 1 |
2008 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2018 | 1 | 0 | 1 |
Below are the most recent publications written about "Ichthyosiform Erythroderma, Congenital" by people in Profiles.
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Juvenile Open Angle Glaucoma With Nonbullous Congenital Ichthyosiform Erythroderma. J Glaucoma. 2018 11; 27(11):e180-e182.
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A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma. Br J Dermatol. 2015 Jan; 172(1):262-4.
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iPS cell modeling of cardiometabolic diseases. J Cardiovasc Transl Res. 2013 Feb; 6(1):46-53.
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Chanarin-Dorfman syndrome with eccrine gland vacuolation: a case report. Int J Dermatol. 2008 Dec; 47(12):1257-9.
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A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrier. J Invest Dermatol. 2007 Aug; 127(8):1893-7.
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Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndrome. Ophthalmology. 2005 Feb; 112(2):e1-6.
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Ichthyosis and keratotic follicular plugs containing dystrophic calcification in newborns: distinctive histopathologic features of x-linked dominant chondrodysplasia punctata (Conradi-Hünermann-Happle syndrome). Am J Dermatopathol. 2004 Feb; 26(1):53-8.
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Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis. Eur J Hum Genet. 1999 Sep; 7(6):625-32.
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The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes. Cell. 1992 Sep 04; 70(5):811-9.