Structured Summary
Abstract
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.
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Synonyms
9 entry terms
- Hyalinosis Cutis et Mucosae
- Lipoidproteinosis
- Lipoproteinosis
- Urbach-Wiethe Disease
- Urbach-Wiethe Lipoid Proteinosis
- Urbach-Wiethe Syndrome
- Lipoid Proteinosis, Urbach-Wiethe
- Urbach Wiethe Disease
- Urbach Wiethe Lipoid Proteinosis
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2007 (1975)
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References
- National Library of Medicine. Lipoid Proteinosis of Urbach and Wiethe. Medical Subject Headings (MeSH). 2026. Unique ID D008065. http://id.nlm.nih.gov/mesh/2026/D008065
- Lipoid Proteinosis of Urbach and Wiethe. In: Wikipedia. https://en.wikipedia.org/wiki/Urbach%E2%80%93Wiethe_disease
- Lipoid Proteinosis of Urbach and Wiethe. In: Wikidata. https://www.wikidata.org/wiki/Q2500124