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.
Follow this condition — get notified about new trialsSub-types
Junctional epidermolysis bullosa, non-Herlitz type
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Epidermolysis bullosa, junctional 2A, intermediate
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Epidermolysis bullosa, junctional 2B, severe
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Epidermolysis bullosa, junctional 3A, intermediate
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Epidermolysis bullosa, junctional 3B, severe
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Epidermolysis bullosa, junctional 4, intermediate
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Epidermolysis bullosa, junctional 5A, intermediate
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Epidermolysis bullosa, junctional 6, with pyloric atresia
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Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
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Generalized junctional epidermolysis bullosa non-Herlitz type
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Junctional epidermolysis bullosa Herlitz type
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Junctional epidermolysis bullosa inversa
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Junctional epidermolysis bullosa with pyloric atresia
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Laryngo-onycho-cutaneous syndrome
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Late-onset junctional epidermolysis bullosa
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Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
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Localized junctional epidermolysis bullosa, non-Herlitz type
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