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Junctional Epidermolysis Bullosa in a Neonate.
Indian pediatrics, 2019 Santhiya, Srinivasan +2 more
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Junctional Epidermolysis Bullosa of the Larynx
Pediatrics, 1986Epidermolysis bullosa is a rare genetically determined, dermatologic disease in which minor trauma causes blister formation.1 A new variant of hereditary epidermolysis bullosa, generalized atrophic benign epidermolysis bullosa, junctional form, has been recently reported.2 Airway involvement has not been a notable feature of this disease. We report the
Sylvan E Stool, Susan B Mallory
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Upper Airway Complications of Junctional Epidermolysis Bullosa
Journal of Pediatrics, 2012To assess the incidence of upper airway pathology in patients with junctional epidermolysis bullosa (JEB).We conducted a retrospective chart review of all patients with JEB who came to an interdisciplinary epidermolysis bullosa center at a tertiary care institution between 2004 and 2010.Twenty-five patients with JEB were identified, and 12 patients ...
Richard G Azizkhan +2 more
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Junctional Epidermolysis Bullosa of the Larynx
Annals of Otology, Rhinology and Laryngology, 1992Epidermolysis bullosa (EB) is a group of rare inherited disorders in which minor trauma causes blister formation in the skin and mucosa, including the esophagus. Morbidity varies with the type of disease and ranges from occasional trivial skin blisters to death in infancy. Laryngeal involvement presenting as hoarseness and respiratory distress has been
Andrew N Lin, D Martin Carter, A N Lin
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Transgenic Epidermal Cultures for Junctional Epidermolysis Bullosa — 5-Year Outcomes
New England Journal of Medicine, 2021 Inherited junctional epidermolysis bullosa is a severe genetic skin disease that leads to epidermal loss caused by structural and mechanical fragility of the integuments. There is no established cure for junctional epidermolysis bullosa.
Michele De Luca, Tobias Hirsch
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Junctional Epidermolysis Bullosa
American Journal of Diseases of Children, 1983Junctional epidermolysis bullosa (EB) is a rare, heritable, blistering disease of the skin characterized by presence of bullae at birth, lack of scarring of the lesions, and early death. To date there has been no effective treatment for the disease. Phenytoin, which decreases collagenase activity in human skin explants and fibroblast cultures, has been
M F, Guill +4 more
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Cicatricial junctional epidermolysis bullosa
Journal of the American Academy of Dermatology, 1985Six types of junctional epidermolysis bullosa (JEB) have been described previously. Each of these types may develop atrophy after recurrent blistering but healing with scar formation does not occur. We describe three cases with a new type of JEB that we have designated as cicatricial junctional epidermolysis bullosa (CJEB).
R M, Haber +3 more
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