 Ichthyosis, Lamellar
"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
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| 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
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| 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
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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 |
|---|
| 1995 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 | | 2018 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 | | 2022 | 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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Sun Q, Asch S, Bayart C, Bayliss SJ, Benjamin L, Bruckner A, DiGiovanna JJ, Fleckman P, Funk T, Lucky A, Nelson CA, Newell B, Polcari I, Teng J, Williams ML, Gan G, Deng Y, Paller AS, Choate KA. Development and Initial Validation of a Novel System to Assess Ichthyosis Severity. JAMA Dermatol. 2022 04 01; 158(4):359-365.
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Zaenglein AL, Levy ML, Stefanko NS, Benjamin LT, Bruckner AL, Choate K, Craiglow BG, DiGiovanna JJ, Eichenfield LF, Elias P, Fleckman P, Lawley LP, Lewis RA, Lucky AW, Mathes EF, Milstone LM, Paller AS, Patel SS, Siegel DH, Teng J, Tanumihardjo SA, Thaxton L, Williams ML. 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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Abboud JJ, Whittington A, Ahmed M, Himebaugh JT, Wiley LA, Haffar A, Nguyen J. Apremilast Use in a Case of Cicatricial Ectropion Secondary to Severe Lamellar Ichthyosis. Ophthalmic Plast Reconstr Surg. 2018 May/Jun; 34(3):e76-e77.
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Shah K, Mehmood S, Jan A, Abbe I, Hussain Ali R, Khan A, Chishti MS, Lee K, Ahmad F, Ansar M, Shahzad S, Nickerson DA, Bamshad MJ, Coucke PJ, Santos-Cortez RLP, Spritz RA, Leal SM, Ahmad W. 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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Zhang L, Ferreyros M, Feng W, Hupe M, Crumrine DA, Chen J, Elias PM, Holleran WM, Niswander L, Hohl D, Williams T, Torchia EC, Roop DR. Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis. PLoS One. 2016; 11(8):e0161465.
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Ullah R, Ansar M, Durrani ZU, Lee K, Santos-Cortez RL, Muhammad D, Ali M, Zia M, Ayub M, Khan S, Smith JD, Nickerson DA, Shendure J, Bamshad M, Leal SM, Ahmad W. Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis. Int J Dermatol. 2016 May; 55(5):524-30.
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Prado R, Ellis LZ, Gamble R, Funk T, Arbuckle HA, Bruckner AL. Collodion baby: an update with a focus on practical management. J Am Acad Dermatol. 2012 Dec; 67(6):1362-74.
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Roop D. Defects in the barrier. Science. 1995 Jan 27; 267(5197):474-5.
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