"Ichthyosis, Lamellar" 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.
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.
| Descriptor ID |
D017490
|
| MeSH Number(s) |
C16.131.831.512.400.410 C16.320.850.400.410 C16.614.492.400.410 C17.800.428.333.250.410 C17.800.804.512.400.410 C17.800.827.400.410
|
| Concept/Terms |
Ichthyosis, Lamellar- Ichthyosis, Lamellar
- Ichthyoses, Lamellar
- Lamellar Ichthyoses
- Congenital Nonbullous Ichthyosiform Erythroderma
- Nonbullous Congenital Lamellar Ichthyosis
- Ichthyosiform Erythroderma, Nonbullous Congenital
- Nonbullous Congenital Ichthyosiform Erythroderma
- Congenital Ichthyosiform Erythroderma, Nonbullous
- Erythroderma Ichthyosiforme, Nonbullous
- Erythroderma Ichthyosiformes, Nonbullous
- Ichthyosiforme, Nonbullous Erythroderma
- Ichthyosiformes, Nonbullous Erythroderma
- Nonbullous Erythroderma Ichthyosiforme
- Nonbullous Erythroderma Ichthyosiformes
Harlequin Fetus- Harlequin Fetus
- Fetus, Harlequin
- Harlequin Ichthyosis
- Harlequin Ichthyoses
- Ichthyoses, Harlequin
- Ichthyosis, Harlequin
|
Below are MeSH descriptors whose meaning is more general than "Ichthyosis, Lamellar".
- 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]
- Ichthyosis, Lamellar [C16.131.831.512.400.410]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
- Ichthyosis, Lamellar [C16.320.850.400.410]
- Infant, Newborn, Diseases [C16.614]
- Ichthyosis [C16.614.492]
- Ichthyosiform Erythroderma, Congenital [C16.614.492.400]
- Ichthyosis, Lamellar [C16.614.492.400.410]
- 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]
- Ichthyosis, Lamellar [C17.800.428.333.250.410]
- Skin Abnormalities [C17.800.804]
- Ichthyosis [C17.800.804.512]
- Ichthyosiform Erythroderma, Congenital [C17.800.804.512.400]
- Ichthyosis, Lamellar [C17.800.804.512.400.410]
- Skin Diseases, Genetic [C17.800.827]
- Ichthyosiform Erythroderma, Congenital [C17.800.827.400]
- Ichthyosis, Lamellar [C17.800.827.400.410]
Below are MeSH descriptors whose meaning is more specific than "Ichthyosis, Lamellar".
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Below are the most recent publications written about "Ichthyosis, Lamellar" by people in Profiles.