Junctional 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.
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epidermolysis bullosa dystrophica
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Kindler syndrome
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late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
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junctional epidermolysis bullosa, non-Herlitz type
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junctional epidermolysis bullosa Herlitz type
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junctional epidermolysis bullosa with pyloric atresia
MONDO:0009183