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.
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
- Junctional Epidermolysis Bullosa
- Epidermolysis Bullosa Junctionalis, Severe Nonlethal
- Epidermolysis Bullosa Junctionalis, Disentis Type
- Epidermolysis Bullosa, Generalized Atrophic Benign
Epidermolysis Bullosa Letalis- Epidermolysis Bullosa Letalis
- Bullosa Letali, Epidermolysis
- Bullosa Letalis, Epidermolysis
- Epidermolysis Bullosa Letali
- Letali, Epidermolysis Bullosa
- Letalis, Epidermolysis Bullosa
- Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type
- Lethal Junctional Epidermolysis Bullosa
- Herlitz's Disease
- Disease, Herlitz's
- Herlitzs Disease
- Herlitz-Pearson Type Epidermolysis Bullosa
- Herlitz Pearson Type Epidermolysis Bullosa
- Epidermolysis Bullosa, Junctional, Herlitz Type
- Herlitz Disease
- Disease, Herlitz
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 Harvard Catalyst Profiles by year, and whether "Epidermolysis Bullosa, Junctional" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 1997 | 1 | 0 | 1 |
| 1998 | 2 | 1 | 3 |
| 2008 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
Below are the most recent publications written about "Epidermolysis Bullosa, Junctional" by people in Profiles.
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A Nonlethal Case of Junctional Epidermolysis Bullosa and Congenital Pyloric Atresia: Compound Heterozygosity in a Patient with a Novel Integrin Beta 4 Gene Mutation. J Pediatr. 2018 02; 193:261-264.e1.
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Neonatal junctional epidermolysis bullosa: treatment conundrums and ethical decision making. Am J Clin Dermatol. 2014 Oct; 15(5):445-50.
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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.
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Junctional epidermolysis bullosa in two domestic shorthair kittens. Vet Dermatol. 2005 Feb; 16(1):69-73.
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Pain management of junctional epidermolysis bullosa in an 11-year-Old boy. Pediatr Dermatol. 1999 Nov-Dec; 16(6):465-8.
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Mutations in extracellular matrix molecules. Curr Opin Cell Biol. 1998 Oct; 10(5):586-93.
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Junctional epidermolysis bullosa: diagnosis and management of a patient with the Herlitz variant. J Pediatr Surg. 1998 May; 33(5):756-8.
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Molecular basis of non-lethal junctional epidermolysis bullosa: identification of a 38 basepair insertion and a splice site mutation in exon 14 of the LAMB3 gene. Exp Dermatol. 1998 Apr-Jun; 7(2-3):105-11.
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Basic fibroblast growth factor: a missing link between collagen VII, increased collagenase, and squamous cell carcinoma in recessive dystrophic epidermolysis bullosa. Mol Med. 1998 Mar; 4(3):191-5.
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Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa. Am J Hum Genet. 1997 Sep; 61(3):611-9.