Related MeSH Hierarchy (6)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Ichthyosis » Ichthyosiform Erythroderma, Congenital » Ichthyosis, Lamellar
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Ichthyosiform Erythroderma, Congenital » Ichthyosis, Lamellar
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Infant, Newborn, Diseases » Ichthyosis » Ichthyosiform Erythroderma, Congenital » Ichthyosis, Lamellar
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Keratosis » Ichthyosis » Ichthyosiform Erythroderma, Congenital » Ichthyosis, Lamellar
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ichthyosis » Ichthyosiform Erythroderma, Congenital » Ichthyosis, Lamellar
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ichthyosiform Erythroderma, Congenital » Ichthyosis, Lamellar
Description
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. MeSH
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Phase 3 Indicated Drugs (1)
Phase 2 Indicated Drugs (2)
Organization Involved with Phase 3 Indications (3)
Organization Involved with Phase 2 Indications (10)
Organization Involved with Phase 1 Indications (1)
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UMLS Data
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