What’s the resolutive surgery for pseudo-ainhum in Vohwinkel syndrome? A case report and review of the literature

Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant autosomal keratosis. It typically presents with “starfish” keratoses on the knuckles, palmoplantar keratoderma (PPK), hearing impairment and mutilating digital constriction bands (pseudoainhum) that ca...

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Detalhes bibliográficos
Publicado no:Orthop Rev (Pavia)
Main Authors: Rovere, Giuseppe, Stramazzo, Leonardo, Cioffi, Alessio, Galvano, Nicolò, Pavan, Davide, Restuccia, Giuseppe, D’Arienzo, Antonio, Capanna, Rodolfo, Maccauro, Giulio, D’Arienzo, Michele, Camarda, Lawrence
Formato: Artigo
Idioma:Inglês
Publicado em: PAGEPress Publications, Pavia, Italy 2021
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7883105/
https://ncbi.nlm.nih.gov/pubmed/33633820
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/or.2020.8868
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