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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
Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Ichthyosis > Ichthyosiform Erythroderma, Congenital
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Ichthyosis > Ichthyosiform Erythroderma, Congenital
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ichthyosis > Ichthyosiform Erythroderma, Congenital
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ichthyosis > Ichthyosiform Erythroderma, Congenital

Terme préférentiel

Ichthyosiform Erythroderma, Congenital  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Concepts spécifiques

Synonyme(s)

  • Congenital Ichthyosiform Erythroderma
  • Erythroderma, Congenital Ichthyosiform

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-B9NRW74T-H

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RDF/XML TURTLE JSON-LD Date de création 12/02/1990, dernière modification le 18/06/2015