Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification

Jo-David Fine (Lead / Corresponding author), Leena Bruckner-Tuderman, Robin A. J. Eady, Eugene A. Bauer, Johann W. Bauer, Cristina Has, Adrian Heagerty, Helmut Hintner, Alain Hovnanian, Marcel F. Jonkman, Irene Leigh, M. Peter Marinkovich, Anna E. Martinez, John A. McGrath, Jemima E. Mellerio, Celia Moss, Dedee F. Murrell, Hiroshi Shimizu, Jouni Uitto, David WoodleyGiovanna Zambruno

    Research output: Contribution to journalArticle

    452 Citations (Scopus)

    Abstract

    Background

    Several new targeted genes and clinical subtypes have been identified since publication in 2008 of the report of the last international consensus meeting on diagnosis and classification of epidermolysis bullosa (EB). As a correlate, new clinical manifestations have been seen in several subtypes previously described.
    Objective

    We sought to arrive at an updated consensus on the classification of EB subtypes, based on newer data, both clinical and molecular.
    Results

    In this latest consensus report, we introduce a new approach to classification (“onion skinning”) that takes into account sequentially the major EB type present (based on identification of the level of skin cleavage), phenotypic characteristics (distribution and severity of disease activity; specific extracutaneous features; other), mode of inheritance, targeted protein and its relative expression in skin, gene involved and type(s) of mutation present, and–when possible–specific mutation(s) and their location(s).
    Limitations

    This classification scheme critically takes into account all published data through June 2013. Further modifications are likely in the future, as more is learned about this group of diseases.
    Conclusion

    The proposed classification scheme should be of value both to clinicians and researchers, emphasizing both clinical and molecular features of each EB subtype, and has sufficient flexibility incorporated in its structure to permit further modifications in the future.
    Original languageEnglish
    Pages (from-to)1103-1126
    Number of pages24
    JournalJournal of the American Academy of Dermatology
    Volume70
    Issue number6
    Early online date29 Mar 2014
    DOIs
    Publication statusPublished - Jun 2014

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  • Cite this

    Fine, J-D., Bruckner-Tuderman, L., Eady, R. A. J., Bauer, E. A., Bauer, J. W., Has, C., Heagerty, A., Hintner, H., Hovnanian, A., Jonkman, M. F., Leigh, I., Marinkovich, M. P., Martinez, A. E., McGrath, J. A., Mellerio, J. E., Moss, C., Murrell, D. F., Shimizu, H., Uitto, J., ... Zambruno, G. (2014). Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. Journal of the American Academy of Dermatology, 70(6), 1103-1126. https://doi.org/10.1016/j.jaad.2014.01.903