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.
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.
| Descriptor ID |
D008065
|
| MeSH Number(s) |
C08.618.490.500 C16.320.850.595
|
| Concept/Terms |
Lipoid Proteinosis of Urbach and Wiethe- Lipoid Proteinosis of Urbach and Wiethe
- Lipoidproteinosis
- Urbach-Wiethe Syndrome
- Urbach-Wiethe Disease
- Urbach Wiethe Disease
- Urbach-Wiethe Lipoid Proteinosis
- Lipoid Proteinosis, Urbach-Wiethe
- Urbach Wiethe Lipoid Proteinosis
- Hyalinosis Cutis et Mucosae
- Lipoproteinosis
|
Below are MeSH descriptors whose meaning is more general than "Lipoid Proteinosis of Urbach and Wiethe".
Below are MeSH descriptors whose meaning is more specific than "Lipoid Proteinosis of Urbach and Wiethe".
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Below are the most recent publications written about "Lipoid Proteinosis of Urbach and Wiethe" by people in Profiles.
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Lipoid proteinosis: case report. Pediatr Dermatol. 1992 Sep; 9(3):264-7.