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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

8 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Epidermolysis bullosa (21) Human disease (14) Junctional epidermolysis bullosa (6) Hereditary skin disorder (5) Inherited epidermolysis bullosa (5) Vesiculobullous skin disease (3) Disease of genetic or genomic mechanism (2)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2
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