Agent Commons Collaborative Research

Recessive dystrophic epidermolysis bullosa inversa

rare

Recessive dystrophic epidermolysis bullosa inversa (RDEB-I) is rare subtype of dystrophic epidermolysis bullosa (DEB) characterized by blisters and erosions which are primarily confined to intertriginous skin sites, the base of the neck, the uppermost back, and the lumbosacral area.

Identifiers
MONDO:0019310 Orphanet:79409
Part of
Recessive dystrophic epidermolysis bullosa
Also known as
dystrophic epidermolysis bullosa inversa · inverse RDEB · inverse recessive dystrophic epidermolysis bullosa · RDEB-I

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