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.
Comprehensive, easy-to-understand information about this condition
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epidermolysis bullosa dystrophica
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epidermolysis bullosa simplex 1A, generalized severe
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epidermolysis bullosa simplex 1C, localized
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epidermolysis bullosa simplex 1B, generalized intermediate
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epidermolysis bullosa simplex 5A, Ogna type
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epidermolysis bullosa simplex 2F, with mottled pigmentation
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