Related MeSH Hierarchy (6)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Ichthyosis » Ichthyosiform Erythroderma, Congenital
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Ichthyosiform Erythroderma, Congenital
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Infant, Newborn, Diseases » Ichthyosis » Ichthyosiform Erythroderma, Congenital
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Keratosis » Ichthyosis » Ichthyosiform Erythroderma, Congenital
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ichthyosis » Ichthyosiform Erythroderma, Congenital
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ichthyosiform Erythroderma, Congenital
Description
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. MeSH
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Subtype Terms (3)
Hyperkeratosis, Epidermolytic
1 approved drug
Ichthyosis, Lamellar
4 drugs (3 approved, 1 experimental)
Netherton Syndrome
10 drugs (4 approved, 6 experimental)
Phase 2 Indicated Drugs (1)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (1)
Organization Involved with Phase 2 Indications (7)
Organization Involved with Other Experimental Indications (3)
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UMLS Data
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