"Epidermolysis Bullosa" 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.
Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.
| Descriptor ID |
D004820
|
| MeSH Number(s) |
C16.131.831.493 C16.320.850.275 C17.800.804.493 C17.800.827.275 C17.800.865.410
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa".
Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa".
This graph shows the total number of publications written about "Epidermolysis Bullosa" by people in this website by year, and whether "Epidermolysis Bullosa" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 0 | 1 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Epidermolysis Bullosa" by people in Profiles.
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The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review. BMC Oral Health. 2024 Sep 27; 24(1):1131.
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Dual mechanism of type VII collagen transfer by bone marrow mesenchymal stem cell extracellular vesicles to recessive dystrophic epidermolysis bullosa fibroblasts. Biochimie. 2018 Dec; 155:50-58.
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Dental care of patients with autoimmune vesiculobullous diseases: case reports and literature review. Quintessence Int. 2006 Nov-Dec; 37(10):777-87.