Epidermolysis Bullosa Simplex

A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex.

Also Known As:

Epidermolysis Bullosa Herpetiformis Dowling Meara; Epidermolysis Bullosa Simplex, Generalized; Epidermolysis Bullosa Simplex, Localized; Weber Cockayne Syndrome; Epidermolysis Bullosa Herpetiformis Dowling-Meara; Epidermolysis Bullosa Simplex Kobner; Weber-Cockayne Syndrome

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Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 449

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Congenital Abnormalities: 10008

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Skin Abnormalities: 78

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Epidermolysis Bullosa: 383

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Epidermolysis Bullosa Simplex: 224

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Inborn Genetic Diseases: 578

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Genetic Skin Diseases: 11

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Epidermolysis Bullosa: 383

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Epidermolysis Bullosa Simplex: 224

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Skin and Connective Tissue Diseases

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Skin Diseases: 6187

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Vesiculobullous Skin Diseases: 223

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Epidermolysis Bullosa: 383

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Epidermolysis Bullosa Simplex: 224

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Skin Abnormalities: 78

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Epidermolysis Bullosa: 383

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Epidermolysis Bullosa Simplex: 224

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Genetic Skin Diseases: 11

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Epidermolysis Bullosa: 383

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Epidermolysis Bullosa Simplex: 224

Katsushi Owaribe Selected Research

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