 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
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| 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
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| 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
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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 |
|---|
| 1999 | 0 | 1 | 1 | | 2001 | 1 | 0 | 1 | | 2004 | 0 | 1 | 1 | | 2014 | 0 | 1 | 1 | | 2017 | 0 | 1 | 1 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Epidermolysis Bullosa Simplex" by people in Profiles.
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Teng J, Paller AS, Bruckner AL, Murrell DF, Mellerio JE, Bodemer C, Martinez AE, Lugo-Somolinos A, Sprecher E, Laimer M, Wally V, Chan YM, Lin SY, Spellman M, Bauer JW. Diacerein 1% Ointment for the Treatment of Epidermolysis Bullosa Simplex: A Randomized, Controlled Trial. J Drugs Dermatol. 2023 06 01; 22(6):599-604.
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Phillips GS, Huang A, Augsburger BD, Kaplan L, Peoples K, Bruckner AL, Khuu P, Tang JY, Lara-Corrales I, Pope E, Wiss K, Levin LE, Morel KD, Hook KP, Paller AS, Eichenfield LF, McCuaig CC, Powell J, Castelo-Soccio L, Levy ML, Price HN, Schachner LA, Browning JC, Jahnke M, Shwayder T, Bayliss S, Lucky AW, Glick SA. 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.
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Camors EM, Purevjav E, Jefferies JL, Saffitz JE, Gong N, Ryan TD, Lucky AW, Taylor MD, Sullivan LM, Mestroni L, Towbin JA. Early Lethality Due to a Novel Desmoplakin Variant Causing Infantile Epidermolysis Bullosa Simplex With Fragile Skin, Aplasia Cutis Congenita, and Arrhythmogenic Cardiomyopathy. Circ Genom Precis Med. 2020 04; 13(2):e002800.
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Gonzalez Garcia A, Tutmaher MS, Upadhyayula SR, Sanchez Russo R, Verma S. Novel PLEC gene variants causing congenital myasthenic syndrome. Muscle Nerve. 2019 12; 60(6):E40-E43.
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Shah K, Mehmood S, Jan A, Abbe I, Hussain Ali R, Khan A, Chishti MS, Lee K, Ahmad F, Ansar M, Shahzad S, Nickerson DA, Bamshad MJ, Coucke PJ, Santos-Cortez RLP, Spritz RA, Leal SM, Ahmad W. Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. Int J Dermatol. 2017 Dec; 56(12):1406-1413.
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Schwieger-Briel A, Chakkittakandiyil A, Lara-Corrales I, Aujla N, Lane AT, Lucky AW, Bruckner AL, Pope E. Instrument for scoring clinical outcome of research for epidermolysis bullosa: a consensus-generated clinical research tool. Pediatr Dermatol. 2015 Jan-Feb; 32(1):41-52.
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Arin MJ, Roop DR. Inducible mouse models for inherited skin diseases: implications for skin gene therapy. Cells Tissues Organs. 2004; 177(3):160-8.
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Cao T, Longley MA, Wang XJ, Roop DR. An inducible mouse model for epidermolysis bullosa simplex: implications for gene therapy. J Cell Biol. 2001 Feb 05; 152(3):651-6.
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Bickenbach JR, Roop DR. Transduction of a preselected population of human epidermal stem cells: consequences for gene therapy. Proc Assoc Am Physicians. 1999 May-Jun; 111(3):184-9.
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Klymkowsky MW. Intermediate filaments. Getting under the skin. Nature. 1991 Nov 28; 354(6351):264.
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