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Epidermolysis Bullosa Simplex (Epidermolysis Bullosa Herpetiformis Dowling Meara) Summary

Description: 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; Epidermolysis Bullosa Simplex, Weber-Cockayne Type; Weber-Cockayne Type Epidermolysis Bullosa Simplex Show All >>

Networked: 294 relevant articles (3 outcomes, 11 trials/studies) for this Disease

Key Drugs and Agents for Epidermolysis Bullosa Simplex

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Drugs and Important Biological Agents (IBA) related to treatments:

trimethyloxamine (trimethylamine N-oxide) : 1 outcome in 2 results : IBA
Cyproheptadine (Periactin) : 1 outcome in 1 result : FDA 2
Bufexamac (Jomax) : 1 outcome in 1 result : IBA
Keratins (Keratin) : 7 studies in 115 results : IBA
Keratin-5 (Keratin 5) : 2 studies in 58 results : IBA
Plectin : 1 study in 57 results : IBA
Proteins (Proteins, Gene) : 1 study in 7 results : IBA
Keratin-1 : 1 study in 2 results : IBA
Pancreatic Elastase (Elastase) : 1 study in 1 result : IBA
Carrier Proteins (Binding Protein) : 1 study in 1 result : IBA

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Diseases Related to Epidermolysis Bullosa Simplex

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Key Therapies for Epidermolysis Bullosa Simplex

Efficacy Chart >>