Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Término preferido
Ichthyosis, Lamellar
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Congenital Ichthyosiform Erythroderma, Nonbullous
- Congenital Nonbullous Ichthyosiform Erythroderma
- Erythroderma Ichthyosiforme, Nonbullous
- Ichthyoses, Lamellar
- Ichthyosiform Erythroderma, Nonbullous Congenital
- Lamellar Ichthyoses
- Lamellar Ichthyosis
- Nonbullous Congenital Ichthyosiform Erythroderma
- Nonbullous Congenital Lamellar Ichthyosis
En otras lenguas
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francés
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Bébé collodion
-
Érythrodermie ichtyosiforme congénitale non bulleuse
-
Érythrodermie ichtyosiforme non bulleuse
URI
http://data.loterre.fr/ark:/67375/JVR-FS4Z13WZ-3
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