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Epidermolysis bullosa simplex

Epidermolysis bullosa simplex (EBS) is a group of hereditary epidermolysis bullosa (HEB) disorders characterized by skin fragility resulting in intraepidermal blisters and erosions that occur either spontaneously or after physical trauma.

5 trials tagged with this condition →

Epidermolysis bullosa simplex 1B, generalized intermediate 1 trial
Epidermolysis bullosa simplex 1A, generalized severe 0 trials
Epidermolysis bullosa simplex 1C, localized 0 trials
Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive 0 trials
Epidermolysis bullosa simplex 2A, generalized severe 0 trials
Epidermolysis bullosa simplex 2B, generalized intermediate 0 trials
Epidermolysis bullosa simplex 2C, localized 0 trials
Epidermolysis bullosa simplex 2E, with migratory circinate erythema 0 trials
Epidermolysis bullosa simplex 2F, with mottled pigmentation 0 trials
Epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive 0 trials
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency 0 trials
Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive 0 trials
Epidermolysis bullosa simplex 5A, Ogna type 0 trials
Epidermolysis bullosa simplex 5B, with muscular dystrophy 0 trials
Epidermolysis bullosa simplex 5C, with pyloric atresia 0 trials
Epidermolysis bullosa simplex 6, generalized, with scarring and hair loss 0 trials
Epidermolysis bullosa simplex 7, with nephropathy and deafness 0 trials
Epidermolysis bullosa simplex with anodontia/hypodontia 0 trials
Epidermolysis bullosa simplex with nail dystrophy 0 trials
Suprabasal epidermolysis bullosa simplex 0 trials Sub-types →