TY - JOUR
T1 - Palmoplantar epidermal differentiation disorders
T2 - a new classification towards pathogenesis-based therapy
AU - Sprecher, Eli
AU - Ishida-Yamamoto, Akemi
AU - Schwartz, Janice
AU - Akiyama, Masashi
AU - Aldwin-Easton, Mandy
AU - Choate, Keith
AU - Fischer, Judith
AU - Gostynski, Antoni
AU - Granier Tournier, Céline
AU - Hernandez-Martin, Angela
AU - Hovnanian, Alain
AU - Malovitski, Kiril
AU - Mazereeuw-Hautier, Juliette
AU - Paller, Amy S
AU - Schmuth, Matthias
AU - Tadini, Gianluca
AU - Teng, Joyce
AU - Bodemer, Christine
AU - O'Toole, Edel A
PY - 2025/3/19
Y1 - 2025/3/19
N2 - More than 50 palmoplantar epidermal differentiation disorders (pEDDs) have been reported in the literature. Various descriptors have been used to name these conditions including clinical features often designated as acronyms or evocative terms, names of clinicians and of geographical locations. Not only has this nomenclature been criticized for its lack of methodological consistency, it has progressively lost its clinical relevance. Indeed, the advent of a wide range of pathogenesis-targeting therapeutic solutions for these disorders has raised the need for a novel classification of pEDDs, based on their causative genetic defects, to provide clinicians with genuine therapeutic guidance. Here, we present a novel classification scheme for pEDDs and its application in the form of a practical algorithm for the rapid diagnosis of pEDDs.
AB - More than 50 palmoplantar epidermal differentiation disorders (pEDDs) have been reported in the literature. Various descriptors have been used to name these conditions including clinical features often designated as acronyms or evocative terms, names of clinicians and of geographical locations. Not only has this nomenclature been criticized for its lack of methodological consistency, it has progressively lost its clinical relevance. Indeed, the advent of a wide range of pathogenesis-targeting therapeutic solutions for these disorders has raised the need for a novel classification of pEDDs, based on their causative genetic defects, to provide clinicians with genuine therapeutic guidance. Here, we present a novel classification scheme for pEDDs and its application in the form of a practical algorithm for the rapid diagnosis of pEDDs.
U2 - 10.1093/bjd/ljaf054
DO - 10.1093/bjd/ljaf054
M3 - Article
SN - 0007-0963
JO - British Journal of Dermatology
JF - British Journal of Dermatology
ER -