"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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 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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Novel compound heterozygous and homozygous variants of laminin subunit ?3 gene underlie non-Herlitz junctional epidermolysis bullosa in two paternal half-brothers from Saudi Arabia. Congenit Anom (Kyoto). 2019 May; 59(3):99-101.
MeSH information
