Concept information
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Preferred term
Ichthyosis, Lamellar
Type
-
Topical Descriptor
Broader concept
Entry terms
- Congenital Ichthyosiform Erythroderma, Nonbullous
- Congenital Nonbullous Ichthyosiform Erythroderma
- Erythroderma Ichthyosiforme, Nonbullous
- Erythroderma Ichthyosiformes, Nonbullous
- Ichthyose, Lamellar
- Ichthyoses, Lamellar
- Ichthyosiforme, Nonbullous Erythroderma
- Ichthyosiform Erythroderma, Nonbullous Congenital
- Ichthyosiformes, Nonbullous Erythroderma
- Lamellar Ichthyose
- Lamellar Ichthyoses
- Lamellar Ichthyosis
- Nonbullous Congenital Ichthyosiform Erythroderma
- Nonbullous Congenital Lamellar Ichthyosis
- Nonbullous Erythroderma Ichthyosiforme
- Nonbullous Erythroderma Ichthyosiformes
Note
- do not coord with INFANT, NEWBORN, DISEASES
Scope note
- A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate.
History note
- 1993; use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992; ERYTHRODERMA ICHTHYOSIFORME, NONBULLOUS use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992, use ICHTHYOSIS 1979-1990
In other languages
-
Finnish
-
ichthyosis congenita lamellaris
-
ichthyosis lamellaris
-
lamellaarinen iktyoosi
-
Swedish
URI
http://www.yso.fi/onto/mesh/D017490
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