"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
- Congenital Nonbullous Ichthyosiform Erythroderma
- Nonbullous Congenital Ichthyosiform Erythroderma
- Ichthyosiform Erythroderma, Nonbullous Congenital
- Lamellar Ichthyoses
- Erythroderma Ichthyosiforme, Nonbullous
- Erythroderma Ichthyosiformes, Nonbullous
- Ichthyosiforme, Nonbullous Erythroderma
- Ichthyosiformes, Nonbullous Erythroderma
- Nonbullous Erythroderma Ichthyosiforme
- Nonbullous Erythroderma Ichthyosiformes
- Congenital Ichthyosiform Erythroderma, Nonbullous
- Lamellar Ichthyosis
- Ichthyoses, Lamellar
- Ichthyose, Lamellar
- Lamellar Ichthyose
- Nonbullous Congenital Lamellar Ichthyosis
Ichthyosis Congenita II- Ichthyosis Congenita II
- Congenita II, Ichthyosis
- Congenita IIs, Ichthyosis
- Ichthyosis Congenita IIs
Ichthyosis Congenita I- Ichthyosis Congenita I
- Congenita I, Ichthyosis
- Congenita Is, Ichthyosis
- Ichthyosis Congenita Is
- Is, Ichthyosis Congenita
- Ichthyosis Congenita
- Congenita, Ichthyosis
- Congenitas, Ichthyosis
- Ichthyosis Congenitas
- Lamellar Ichthyosis, Type 1
- Lamellar Exfoliation of Newborn
- Newborn Lamellar Exfoliation
- Newborn Lamellar Exfoliations
- Ichthyosis, Lamellar, 1
Collodion Fetus- Collodion Fetus
- Fetus, Collodion
- Collodion Baby Syndrome
- Baby Syndrome, Collodion
- Baby Syndromes, Collodion
- Collodion Baby Syndromes
- Syndrome, Collodion Baby
- Syndromes, Collodion Baby
- Desquamation of Newborn
- Newborn Desquamation
- Newborn Desquamations
Harlequin Fetus- Harlequin Fetus
- Fetus, Harlequin
- Harlequin Baby Syndrome
- Baby Syndrome, Harlequin
- Baby Syndromes, Harlequin
- Harlequin Baby Syndromes
- Syndrome, Harlequin Baby
- Syndromes, Harlequin Baby
- 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".
This graph shows the total number of publications written about "Ichthyosis, Lamellar" by people in this website by year, and whether "Ichthyosis, Lamellar" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Ichthyosis, Lamellar" by people in Profiles.
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In-person validation of the Ichthyosis Scoring System. Pediatr Dermatol. 2024 Mar-Apr; 41(2):247-252.
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Interleukin-18 as a severity marker and novel potential therapeutic target for epidermolytic ichthyosis. Clin Exp Dermatol. 2023 Mar 01; 48(3):199-210.
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Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug-induced associations. J Eur Acad Dermatol Venereol. 2023 Jan; 37(1):47-56.
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Consensus recommendations for the use of retinoids in ichthyosis and other disorders of cornification in children and adolescents. Pediatr Dermatol. 2021 Jan; 38(1):164-180.
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Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis. Br J Dermatol. 2020 03; 182(3):729-737.
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Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families. Hum Mutat. 2019 03; 40(3):288-298.
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Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. Int J Dermatol. 2017 Dec; 56(12):1406-1413.
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Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity. J Invest Dermatol. 2017 03; 137(3):678-685.
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Gaucher Disease Type 2 Presenting with Collodion Membrane and Blueberry Muffin Lesions. Pediatr Dermatol. 2016 Jan-Feb; 33(1):e20-2.
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Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis. Int J Dermatol. 2016 May; 55(5):524-30.