Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Preferred term
Ichthyosiform Erythroderma, Congenital
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Congenital Ichthyosiform Erythroderma
- Congenital Ichthyosiform Erythrodermas
- Erythroderma, Congenital Ichthyosiform
- Erythrodermas, Congenital Ichthyosiform
- Ichthyosiform Erythrodermas, Congenital
Note
- an ichthyosis rather than an erythroderma; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Scope note
- 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.
History note
- 91
In other languages
-
Finnish
-
erythrodermia ichthyosiformis
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erythrodermia ichthyosiformis bullosa
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erythrodermia ichthyosiformis congenita
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kongenitaalinen iktyoosiforminen erytroderma
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synnynnäinen iktyoosiforminen erytroderma
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synnynnäinen rakkulainen iktyoosin kaltainen erytrodermia
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Swedish
URI
http://www.yso.fi/onto/mesh/D016113
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