Junctional epidermolysis bullosa inversa

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Junctional epidermolysis bullosa inversa

Synonyms: JEB inversa | JEB-I

A rare intermediate form of junctional epidermolysis bullosa characterized by congenital blistering and erosions confined to intertriginous skin sites the esophagus groin and perineum. Blistering is usually severe and lesions may heal with atrophic scarring and milia formation. Extracutaneous manifestations include nail dystrophy enamel hypoplasia and dental caries oral esophageal and vaginal blisters and erosions.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024

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Junctional epidermolysis bullosa inversa?

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