Junctional epidermolysis bullosa inversa

MONDO:0019308

Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa (JEB) characterized by blistering and erosions confined to intertriginous skin sites, the esophagus, and vagina.

Also known as: EBJ-I, JEB-I, inverse JEB

1 clinical trial for this condition and its sub-types, 0 tagged with Junctional epidermolysis bullosa inversa itself.

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↑ Junctional epidermolysis bullosa (8)

Including sub-types (1) Tagged with Junctional epidermolysis bullosa inversa (0)

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