Junctional epidermolysis bullosa
MONDO:0017612Junctional epidermolysis bullosa (JEB) is a form of inherited epidermolysis bullosa characterized by involvement of the skin and mucous membranes, and is defined by the formation of blistering lesions between the epidermis and the dermis at the lamina lucida level of the cutaneous basement membrane zone and by healing of lesions with atrophy and/or exuberant granulation tissue formation.
Also known as: EBJ, JEB, epidermolysis bullosa atrophicans, junctional epidermolysis bullosa, epidermolysis bullosa hereditaria letalis, epidermolysis bullosa, junctional
9 clinical trials for this condition and its sub-types, 6 tagged with Junctional epidermolysis bullosa itself.
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Browse by category →Sub-types of Junctional epidermolysis bullosa
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2 sub-types
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Laryngo-onycho-cutaneous syndrome 0 trials