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Ichthyosis

"Ichthyosis" 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.

expand / collapse MeSH information
Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome.


expand / collapse Publications
This graph shows the total number of publications written about "Ichthyosis" by people in this website by year, and whether "Ichthyosis" was a major or minor topic of these publications.
Below are the most recent publications written about "Ichthyosis" by people in Profiles.
  1. Identification of a novel partial deletion of STS associated with pre-Descemet corneal dystrophy and X-linked ichthyosis. Mol Vis. 2023; 29:25-30.
    View in: PubMed
  2. A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis. PLoS One. 2022; 17(10):e0275367.
    View in: PubMed
  3. Development and Initial Validation of a Novel System to Assess Ichthyosis Severity. JAMA Dermatol. 2022 04 01; 158(4):359-365.
    View in: PubMed
  4. Executive summary: Consensus recommendations for the use of retinoids in ichthyosis and other disorders of cornification in children and adolescents. J Am Acad Dermatol. 2022 01; 86(1):158-161.
    View in: PubMed
  5. Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support a Specific Role in Lipid-Protein Cross-Linking. Am J Pathol. 2021 05; 191(5):921-929.
    View in: PubMed
  6. 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.
    View in: PubMed
  7. Limbal Stem Cell Dysfunction in Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome. Cornea. 2020 Oct; 39(10):1321-1324.
    View in: PubMed
  8. Proteomic manifestations of genetic defects in autosomal recessive congenital ichthyosis. J Proteomics. 2019 06 15; 201:104-109.
    View in: PubMed
  9. A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype. J Clin Immunol. 2019 04; 39(3):249-256.
    View in: PubMed
  10. Keratosis Pilaris and its Subtypes: Associations, New Molecular and Pharmacologic Etiologies, and Therapeutic Options. Am J Clin Dermatol. 2018 Oct; 19(5):733-757.
    View in: PubMed