Ichthyosiform Erythroderma, Congenital

"Ichthyosiform Erythroderma, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D016113
MeSH Number(s)	C16.131.831.512.400 C16.320.850.400 C16.614.492.400 C17.800.428.333.250 C17.800.804.512.400 C17.800.827.400
Concept/Terms	Ichthyosiform Erythroderma, Congenital Ichthyosiform Erythroderma, Congenital Erythroderma, Congenital Ichthyosiform Congenital Ichthyosiform Erythrodermas Erythrodermas, Congenital Ichthyosiform Ichthyosiform Erythrodermas, Congenital Congenital Ichthyosiform Erythroderma Congenital Ichthyosiform Erythroderma, Wet Type Congenital Ichthyosiform Erythroderma, Wet Type Congenital Ichthyosiform Erythroderma, Dry Type Congenital Ichthyosiform Erythroderma, Dry Type

Below are MeSH descriptors whose meaning is more general than "Ichthyosiform Erythroderma, Congenital".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Ichthyosis [C16.131.831.512]
Ichthyosiform Erythroderma, Congenital [C16.131.831.512.400]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
Infant, Newborn, Diseases [C16.614]
Ichthyosis [C16.614.492]
Ichthyosiform Erythroderma, Congenital [C16.614.492.400]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Keratosis [C17.800.428]
Ichthyosis [C17.800.428.333]
Ichthyosiform Erythroderma, Congenital [C17.800.428.333.250]
Skin Abnormalities [C17.800.804]
Ichthyosis [C17.800.804.512]
Ichthyosiform Erythroderma, Congenital [C17.800.804.512.400]
Skin Diseases, Genetic [C17.800.827]
Ichthyosiform Erythroderma, Congenital [C17.800.827.400]

Below are MeSH descriptors whose meaning is related to "Ichthyosiform Erythroderma, Congenital".

Below are MeSH descriptors whose meaning is more specific than "Ichthyosiform Erythroderma, Congenital".

publications

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