Phenytoin Therapy for Junctional Epidermolysis Bullosa

R. B. Rogers, K. B. Yancey, B. S. Allen, M. F. Guill

Research output: Contribution to journalArticle

12 Scopus citations

Abstract

Junctional epidermolysis bullosa (JEB) is a recessively inherited mechanobullous disease characterized by neonatal onset of blisters, healing without scarring or milium formation, dystrophic nails, and internal involvement in some patients. Several treatment modalities have been tried, including systemic corticosteroids and oral vitamin E, but no form of therapy has been uniformly successful. We describe a patient with JEB treated with phenytoin, followed by improvement in his skin lesions.

Original languageEnglish (US)
Pages (from-to)925-926
Number of pages2
JournalArchives of Dermatology
Volume119
Issue number11
DOIs
StatePublished - Nov 1983

ASJC Scopus subject areas

  • Dermatology

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