Epidermolysis Bullosa Simplex
"Epidermolysis Bullosa Simplex" 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.
A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex.
| Descriptor ID |
D016110
|
| MeSH Number(s) |
C16.131.831.493.180 C16.320.850.275.180 C17.800.804.493.180 C17.800.827.275.180 C17.800.865.410.180
|
| Concept/Terms |
Epidermolysis Bullosa Simplex Kobner- Epidermolysis Bullosa Simplex Kobner
- Epidermolysis Bullosa Simplex, Generalized
- Epidermolysis Bullosa Simplex, Koebner Type
- EBS, Generalized
- EBSs, Generalized
- Generalized EBS
- Generalized EBSs
Weber-Cockayne Syndrome- Weber-Cockayne Syndrome
- Weber Cockayne Syndrome
- EBS, Acral Form
- Acral Form EBS
- Acral Form EBSs
- EBSs, Acral Form
- Epidermolysis Bullosa Simplex, Cockayne-Touraine Type
- Epidermolysis Bullosa Simplex, Cockayne Touraine Type
- Epidermolysis Bullosa Simplex, Weber-Cockayne Type
- Epidermolysis Bullosa Simplex, Weber Cockayne Type
- Epidermolysis Bullosa Simplex, Localized
- Weber-Cockayne Type Epidermolysis Bullosa Simplex
- Weber Cockayne Type Epidermolysis Bullosa Simplex
- Epidermolysis Bullosa of Hands and Feet
Epidermolysis Bullosa Herpetiformis Dowling-Meara- Epidermolysis Bullosa Herpetiformis Dowling-Meara
- Epidermolysis Bullosa Simplex, Dowling-Meara Type
- Epidermolysis Bullosa Simplex, Dowling Meara Type
- EBS-DM
- Epidermolysis Bullosa Herpetiformis Dowling Meara
- Epidermolysis Bullosa Herpetiformis, Dowling-Meara
- Epidermolysis Bullosa Herpetiformis, Dowling Meara
- Epidermolysis Bullosa Herpetiformis, Dowling-Meara Type
- Epidermolysis Bullosa Herpetiformis, Dowling Meara Type
|
Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa Simplex".
Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa Simplex".
This graph shows the total number of publications written about "Epidermolysis Bullosa Simplex" by people in this website by year, and whether "Epidermolysis Bullosa Simplex" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Epidermolysis Bullosa Simplex" by people in Profiles.
-
A retrospective analysis of diagnostic testing in a large North American cohort of patients with epidermolysis bullosa. J Am Acad Dermatol. 2022 05; 86(5):1063-1071.
-
Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. Int J Dermatol. 2017 Dec; 56(12):1406-1413.
-
Epidermolysis bullosa simplex with mottled pigmentation. Dermatol Online J. 2012 Jan 15; 18(1):9.
-
Successful radiation therapy for supratentorial primitive neuroectodermal tumor and epidermolysis bullosa simplex. Pediatr Blood Cancer. 2010 Jan; 54(1):170-2.
-
Immunohistochemical detection of keratin with the monoclonal antibody MNF116 is useful in the diagnosis of epidermolysis bullosa simplex. J Cutan Pathol. 1994 Apr; 21(2):118-22.