Lipoid Proteinosis of Urbach and Wiethe

"Lipoid Proteinosis of Urbach and Wiethe" 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
An autosomal recessive disorder characterized by glassy degenerative thickening (hyalinosis) of SKIN; MUCOSA; and certain VISCERA. This disorder is caused by mutation in the extracellular matrix protein 1 gene (ECM1). Clinical features include hoarseness and skin eruption due to widespread deposition of HYALIN.


Publications
This graph shows the total number of publications written about "Lipoid Proteinosis of Urbach and Wiethe" by people in this website by year, and whether "Lipoid Proteinosis of Urbach and Wiethe" was a major or minor topic of these publications.
Bar chart showing 3 publications over 3 distinct years, with a maximum of 1 publications in 2017 and 2018 and 2019
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