Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Infant, Newborn, Diseases
Ichthyosis
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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