Cure My Disease

Don't miss your cure!

Log in / Sign up

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.

Follow this condition — get notified about new trials

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

Skin deep: european study probes the hidden emotional toll of skin diseases

Knowledge-focused Not yet recruiting

This study looks at how people with skin conditions (like eczema, psoriasis, or skin cancer) manage stress, feel lonely, and bounce back from challenges. Researchers will compare 375 adults with and without skin disease across 15 European countries using questionnaires. The goal …

Phase: NA • Sponsor: University Hospital, Brest • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:06 UTC