Epidermolysis Bullosa, Junctional
"Epidermolysis Bullosa, Junctional" 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.
Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane.
| Descriptor ID |
D016109
|
| MeSH Number(s) |
C16.131.831.493.170 C16.320.850.275.170 C17.800.804.493.170 C17.800.827.275.170 C17.800.865.410.170
|
| Concept/Terms |
Epidermolysis Bullosa, Junctional- Epidermolysis Bullosa, Junctional
- Epidermolysis Bullosa, Generalized Atrophic Benign
- Epidermolysis Bullosa Junctionalis, Severe Nonlethal
- Junctional Epidermolysis Bullosa
- Epidermolysis Bullosa Junctionalis, Disentis Type
Epidermolysis Bullosa Letalis- Epidermolysis Bullosa Letalis
- Bullosa Letali, Epidermolysis
- Bullosa Letalis, Epidermolysis
- Epidermolysis Bullosa Letali
- Letali, Epidermolysis Bullosa
- Letalis, Epidermolysis Bullosa
- Herlitz Disease
- Disease, Herlitz
- Lethal Junctional Epidermolysis Bullosa
- Herlitz-Pearson-Type Epidermolysis Bullosa
- Bullosa, Herlitz-Pearson-Type Epidermolysis
- Epidermolysis Bullosa, Herlitz-Pearson-Type
- Epidermolysis Bullosa, Junctional, Herlitz Type
- Herlitz-Pearson Type Epidermolysis Bullosa
- Herlitz Pearson Type Epidermolysis Bullosa
- Epidermolysis Bullosa Junctionalis, Herlitz Type
- Herlitz's Disease
- Disease, Herlitz's
- Herlitzs Disease
- Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type
|
Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa, Junctional".
- Diseases [C]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Skin Abnormalities [C16.131.831]
- Epidermolysis Bullosa [C16.131.831.493]
- Epidermolysis Bullosa, Junctional [C16.131.831.493.170]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Epidermolysis Bullosa [C16.320.850.275]
- Epidermolysis Bullosa, Junctional [C16.320.850.275.170]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Skin Abnormalities [C17.800.804]
- Epidermolysis Bullosa [C17.800.804.493]
- Epidermolysis Bullosa, Junctional [C17.800.804.493.170]
- Skin Diseases, Genetic [C17.800.827]
- Epidermolysis Bullosa [C17.800.827.275]
- Epidermolysis Bullosa, Junctional [C17.800.827.275.170]
- Skin Diseases, Vesiculobullous [C17.800.865]
- Epidermolysis Bullosa [C17.800.865.410]
- Epidermolysis Bullosa, Junctional [C17.800.865.410.170]
Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa, Junctional".
This graph shows the total number of publications written about "Epidermolysis Bullosa, Junctional" by people in this website by year, and whether "Epidermolysis Bullosa, Junctional" 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 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Epidermolysis Bullosa, Junctional" by people in Profiles.
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Orlowski GM, Amano SU, Flanagan KE, Rieger KE, Marinkovich MP, Wiss K. Treatment With Ataluren for Wound Healing and Health Complications in a Patient With Junctional Epidermolysis Bullosa. JAMA Dermatol. 2023 10 01; 159(10):1145-1147.
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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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Salvestrini C, McGrath JA, Ozoemena L, Husain K, Buhamrah E, Sabery N, Leichtner A, Rufo PA, Perez-Atayde A, Orteu CH, Torrente F, Heuschkel RB, Thomson MA, Murch SH. Desquamative enteropathy and pyloric atresia without skin disease caused by a novel intracellular beta4 integrin mutation. J Pediatr Gastroenterol Nutr. 2008 Nov; 47(5):585-91.